ClinGen Allele Registry
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Canonical Allele Identifier:
CA375686337
Gene: ABO
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr9:g.136131669T>A (hg19)
chr9:g.133256282T>A (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.133256282T>A , CM000671.2:g.133256282T>A
GRCh38
NC_000009.11:g.136131669T>A , CM000671.1:g.136131669T>A
GRCh37
NC_000009.10:g.135121490T>A
NCBI36
NG_006669.1:g.21386A>T
NG_006669.2:g.23934A>T
Transcript Alleles
HGVS
Amino-acid change
ENST00000453660.4:n.478A>T
ENST00000647353.1:n.54-5130A>T
ENST00000651471.1:n.404A>T
ENST00000679909.1:c.28+18880A>T
ENSP00000506089.1:n.28+18880A>T
ENST00000453660.3:n.460A>T
ENST00000538324.2:c.446A>T
ENSP00000483018.1:p.Tyr149Phe
ENST00000611156.4:c.446A>T
ENSP00000483265.1:p.Tyr149Phe
NM_020469.2:c.449A>T
NP_065202.2:p.Tyr150Phe
NM_020469.3:c.449A>T
NP_065202.2:p.Tyr150Phe
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