Canonical Allele Identifier: CA467782209

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131031T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255644T>G , CM000671.2:g.133255644T>G	GRCh38
NC_000009.11:g.136131031T>G , CM000671.1:g.136131031T>G	GRCh37
NC_000009.10:g.135120852T>G	NCBI36
NG_006669.1:g.22024A>C
NG_006669.2:g.24572A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1116A>C
ENST00000647353.1:n.54-4492A>C
ENST00000679909.1:c.28+19518A>C	ENSP00000506089.1:n.28+19518A>C
ENST00000453660.3:n.1098A>C
ENST00000538324.2:c.1080A>C	ENSP00000483018.1:p.Gly360=
ENST00000611156.4:c.*22A>C	ENSP00000483265.1:n.*22A>C
NM_020469.2:c.*22A>C	NP_065202.2:n.*22A>C
NM_020469.3:c.*22A>C	NP_065202.2:n.*22A>C