Canonical Allele Identifier: CA860757313
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1432814683
MyVariant Identifiers: chr9:g.133261789T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133261789T>C , CM000671.2:g.133261789T>C GRCh38
NC_000009.11:g.136137192T>C , CM000671.1:g.136137192T>C GRCh37
NC_000009.10:g.135127013T>C NCBI36
NG_006669.1:g.15861A>G
NG_006669.2:g.18426A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.128+310A>G
ENST00000647353.1:n.54-10637A>G
ENST00000651471.1:n.133+310A>G
ENST00000679909.1:c.28+13373A>G ENSP00000506089.1:n.28+13373A>G
ENST00000453660.3:n.110+310A>G
ENST00000538324.2:c.98+310A>G ENSP00000483018.1:n.98+310A>G
ENST00000611156.4:c.98+310A>G ENSP00000483265.1:n.98+310A>G
NM_020469.2:c.98+310A>G NP_065202.2:n.98+310A>G
NM_020469.3:c.98+310A>G NP_065202.2:n.98+310A>G
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