Canonical Allele Identifier: CA200767697
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs903355334
MyVariant Identifiers: chr9:g.133261747T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133261747T>G , CM000671.2:g.133261747T>G GRCh38
NC_000009.11:g.136137150T>G , CM000671.1:g.136137150T>G GRCh37
NC_000009.10:g.135126971T>G NCBI36
NG_006669.1:g.15903A>C
NG_006669.2:g.18468A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.128+352A>C
ENST00000647353.1:n.54-10595A>C
ENST00000651471.1:n.133+352A>C
ENST00000679909.1:c.28+13415A>C ENSP00000506089.1:n.28+13415A>C
ENST00000453660.3:n.110+352A>C
ENST00000538324.2:c.98+352A>C ENSP00000483018.1:n.98+352A>C
ENST00000611156.4:c.98+352A>C ENSP00000483265.1:n.98+352A>C
NM_020469.2:c.98+352A>C NP_065202.2:n.98+352A>C
NM_020469.3:c.98+352A>C NP_065202.2:n.98+352A>C
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