Canonical Allele Identifier: CA467781397

Gene: ABO

Linked Data

• gnomAD v4: 9-133255528-T-G
• MyVariant Identifiers: chr9:g.136130915T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255528T>G , CM000671.2:g.133255528T>G	GRCh38
NC_000009.11:g.136130915T>G , CM000671.1:g.136130915T>G	GRCh37
NC_000009.10:g.135120736T>G	NCBI36
NG_006669.1:g.22140A>C
NG_006669.2:g.24688A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.1232A>C
ENST00000647353.1:n.54-4376A>C
ENST00000679909.1:c.28+19634A>C	ENSP00000506089.1:n.28+19634A>C
ENST00000453660.3:n.1214A>C
ENST00000611156.4:c.*138A>C	ENSP00000483265.1:n.*138A>C
NM_020469.2:c.*138A>C	NP_065202.2:n.*138A>C
NM_020469.3:c.*138A>C	NP_065202.2:n.*138A>C