Canonical Allele Identifier: CA375685804

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131477A>C (hg19) ; chr9:g.133256090A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256090A>C , CM000671.2:g.133256090A>C	GRCh38
NC_000009.11:g.136131477A>C , CM000671.1:g.136131477A>C	GRCh37
NC_000009.10:g.135121298A>C	NCBI36
NG_006669.1:g.21578T>G
NG_006669.2:g.24126T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.670T>G
ENST00000647353.1:n.54-4938T>G
ENST00000679909.1:c.28+19072T>G	ENSP00000506089.1:n.28+19072T>G
ENST00000453660.3:n.652T>G
ENST00000538324.2:c.638T>G	ENSP00000483018.1:p.Met213Arg
ENST00000611156.4:c.638T>G	ENSP00000483265.1:p.Met213Arg
NM_020469.2:c.641T>G	NP_065202.2:p.Met214Arg
NM_020469.3:c.641T>G	NP_065202.2:p.Met214Arg