Canonical Allele Identifier: CA375685261

Gene: ABO

Linked Data

• gnomAD v4: 9-133255973-T-C
• MyVariant Identifiers: chr9:g.136131360T>C (hg19) ; chr9:g.133255973T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255973T>C , CM000671.2:g.133255973T>C	GRCh38
NC_000009.11:g.136131360T>C , CM000671.1:g.136131360T>C	GRCh37
NC_000009.10:g.135121181T>C	NCBI36
NG_006669.1:g.21695A>G
NG_006669.2:g.24243A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.787A>G
ENST00000647353.1:n.54-4821A>G
ENST00000679909.1:c.28+19189A>G	ENSP00000506089.1:n.28+19189A>G
ENST00000453660.3:n.769A>G
ENST00000538324.2:c.755A>G	ENSP00000483018.1:p.Gln252Arg
ENST00000611156.4:c.755A>G	ENSP00000483265.1:p.Gln252Arg
NM_020469.2:c.758A>G	NP_065202.2:p.Gln253Arg
NM_020469.3:c.758A>G	NP_065202.2:p.Gln253Arg