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AGCAGCCGGATGGTAAGTCTGTGGG[C/T]CCGTCCTCCCTTCGCTGGCCCAGAT
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 602730 MIM: 604051 | |||||||||||||||||||||||
Literature Links: |
ACVR2B PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
ACVR2B - activin A receptor type 2B | ||||||
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There are no transcripts associated with this gene. |
EXOG - endo/exonuclease (5'-3'), endonuclease G-like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145464.1 | Intron | NP_001138936.1 | ||||
NM_001318954.1 | Intron | NP_001305883.1 | ||||
NM_001318955.1 | Intron | NP_001305884.1 | ||||
NM_001318956.1 | Intron | NP_001305885.1 | ||||
NM_001318957.1 | Intron | NP_001305886.1 | ||||
NM_001318958.1 | Intron | NP_001305887.1 | ||||
NM_001318959.1 | Intron | NP_001305888.1 | ||||
NM_005107.3 | Intron | NP_005098.2 | ||||
XM_005265633.3 | Intron | XP_005265690.1 | ||||
XM_005265635.3 | Intron | XP_005265692.1 | ||||
XM_006713442.3 | Intron | XP_006713505.1 | ||||
XM_006713444.3 | Intron | XP_006713507.1 | ||||
XM_017007584.1 | Intron | XP_016863073.1 | ||||
XM_017007585.1 | Intron | XP_016863074.1 | ||||
XM_017007586.1 | Intron | XP_016863075.1 | ||||
XM_017007587.1 | Intron | XP_016863076.1 | ||||
XM_017007588.1 | Intron | XP_016863077.1 | ||||
XM_017007589.1 | Intron | XP_016863078.1 | ||||
XM_017007590.1 | Intron | XP_016863079.1 | ||||
XM_017007591.1 | Intron | XP_016863080.1 | ||||
XM_017007592.1 | Intron | XP_016863081.1 | ||||
XM_017007593.1 | Intron | XP_016863082.1 | ||||
XM_017007594.1 | Intron | XP_016863083.1 |