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ACAGCCTCCCTAAAATGCGCGTGGA[A/G]GCAGCTGGGCCTTTGTCTCCTGGGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 611192 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ANKRD11 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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
|
ANKRD11 - ankyrin repeat domain 11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256182.1 | Intron | NP_001243111.1 | ||||
NM_001256183.1 | Intron | NP_001243112.1 | ||||
NM_013275.5 | Intron | NP_037407.4 | ||||
XM_006721181.1 | Intron | XP_006721244.1 | ||||
XM_006721184.2 | Intron | XP_006721247.1 | ||||
XM_011523051.2 | Intron | XP_011521353.1 | ||||
XM_011523053.2 | Intron | XP_011521355.1 | ||||
XM_011523054.2 | Intron | XP_011521356.1 | ||||
XM_011523055.2 | Intron | XP_011521357.1 | ||||
XM_011523056.2 | Intron | XP_011521358.1 | ||||
XM_011523057.2 | Intron | XP_011521359.1 | ||||
XM_017023182.1 | Intron | XP_016878671.1 | ||||
XM_017023183.1 | Intron | XP_016878672.1 | ||||
XM_017023184.1 | Intron | XP_016878673.1 | ||||
XM_017023185.1 | Intron | XP_016878674.1 | ||||
XM_017023186.1 | Intron | XP_016878675.1 | ||||
XM_017023187.1 | Intron | XP_016878676.1 |