Canonical Allele Identifier: CA375684774

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131268A>G (hg19) ; chr9:g.133255881A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255881A>G , CM000671.2:g.133255881A>G	GRCh38
NC_000009.11:g.136131268A>G , CM000671.1:g.136131268A>G	GRCh37
NC_000009.10:g.135121089A>G	NCBI36
NG_006669.1:g.21787T>C
NG_006669.2:g.24335T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.879T>C
ENST00000647353.1:n.54-4729T>C
ENST00000679909.1:c.28+19281T>C	ENSP00000506089.1:n.28+19281T>C
ENST00000453660.3:n.861T>C
ENST00000538324.2:c.847T>C	ENSP00000483018.1:p.Cys283Arg
ENST00000611156.4:c.847T>C	ENSP00000483265.1:p.Cys283Arg
NM_020469.2:c.850T>C	NP_065202.2:p.Cys284Arg
NM_020469.3:c.850T>C	NP_065202.2:p.Cys284Arg