Canonical Allele Identifier: CA375684389

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131223C>G (hg19) ; chr9:g.133255836C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255836C>G , CM000671.2:g.133255836C>G	GRCh38
NC_000009.11:g.136131223C>G , CM000671.1:g.136131223C>G	GRCh37
NC_000009.10:g.135121044C>G	NCBI36
NG_006669.1:g.21832G>C
NG_006669.2:g.24380G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.924G>C
ENST00000647353.1:n.54-4684G>C
ENST00000679909.1:c.28+19326G>C	ENSP00000506089.1:n.28+19326G>C
ENST00000453660.3:n.906G>C
ENST00000538324.2:c.892G>C	ENSP00000483018.1:p.Val298Leu
ENST00000611156.4:c.892G>C	ENSP00000483265.1:p.Val298Leu
NM_020469.2:c.895G>C	NP_065202.2:p.Val299Leu
NM_020469.3:c.895G>C	NP_065202.2:p.Val299Leu