Canonical Allele Identifier: CA375683958

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131175G>C (hg19) ; chr9:g.133255788G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255788G>C , CM000671.2:g.133255788G>C	GRCh38
NC_000009.11:g.136131175G>C , CM000671.1:g.136131175G>C	GRCh37
NC_000009.10:g.135120996G>C	NCBI36
NG_006669.1:g.21880C>G
NG_006669.2:g.24428C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.972C>G
ENST00000647353.1:n.54-4636C>G
ENST00000679909.1:c.28+19374C>G	ENSP00000506089.1:n.28+19374C>G
ENST00000453660.3:n.954C>G
ENST00000538324.2:c.940C>G	ENSP00000483018.1:p.Pro314Ala
ENST00000611156.4:c.940C>G	ENSP00000483265.1:p.Pro314Ala
NM_020469.2:c.943C>G	NP_065202.2:p.Pro315Ala
NM_020469.3:c.943C>G	NP_065202.2:p.Pro315Ala