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TTTATTTTCATTTTACATATAGTTT[A/G]AAGATATCTCCACACTGGCTCAAAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 114025 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CTNNA2 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
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
CTNNA2 - catenin alpha 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001164883.1 | Intron | NP_001158355.1 | ||||
NM_001282597.2 | Intron | NP_001269526.1 | ||||
NM_001282598.1 | Intron | NP_001269527.1 | ||||
NM_001282599.1 | Intron | NP_001269528.1 | ||||
NM_001282600.1 | Intron | NP_001269529.1 | ||||
NM_001320810.1 | Intron | NP_001307739.1 | ||||
NM_004389.3 | Intron | NP_004380.2 | ||||
XM_011532555.2 | Intron | XP_011530857.1 | ||||
XM_011532556.2 | Intron | XP_011530858.1 | ||||
XM_011532557.2 | Intron | XP_011530859.1 | ||||
XM_017003403.1 | Intron | XP_016858892.1 | ||||
XM_017003404.1 | Intron | XP_016858893.1 | ||||
XM_017003405.1 | Intron | XP_016858894.1 | ||||
XM_017003406.1 | Intron | XP_016858895.1 |