Canonical Allele Identifier: CA375682249

Gene: ABO

Linked Data

• gnomAD v4: 9-133255642-C-T
• MyVariant Identifiers: chr9:g.136131029C>T (hg19) ; chr9:g.133255642C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255642C>T , CM000671.2:g.133255642C>T	GRCh38
NC_000009.11:g.136131029C>T , CM000671.1:g.136131029C>T	GRCh37
NC_000009.10:g.135120850C>T	NCBI36
NG_006669.1:g.22026G>A
NG_006669.2:g.24574G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1118G>A
ENST00000647353.1:n.54-4490G>A
ENST00000679909.1:c.28+19520G>A	ENSP00000506089.1:n.28+19520G>A
ENST00000453660.3:n.1100G>A
ENST00000538324.2:c.1082G>A	ENSP00000483018.1:p.Gly361Glu
ENST00000611156.4:c.*24G>A	ENSP00000483265.1:n.*24G>A
NM_020469.2:c.*24G>A	NP_065202.2:n.*24G>A
NM_020469.3:c.*24G>A	NP_065202.2:n.*24G>A