Canonical Allele Identifier: CA467779949

Gene: ABO

Linked Data

• gnomAD v4: 9-133255293-T-C
• MyVariant Identifiers: chr9:g.136130680T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255293T>C , CM000671.2:g.133255293T>C	GRCh38
NC_000009.11:g.136130680T>C , CM000671.1:g.136130680T>C	GRCh37
NC_000009.10:g.135120501T>C	NCBI36
NG_006669.1:g.22375A>G
NG_006669.2:g.24923A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1467A>G
ENST00000647353.1:n.54-4141A>G
ENST00000679909.1:c.28+19869A>G	ENSP00000506089.1:n.28+19869A>G
ENST00000453660.3:n.1449A>G
ENST00000611156.4:c.*373A>G	ENSP00000483265.1:n.*373A>G
NM_020469.2:c.*373A>G	NP_065202.2:n.*373A>G
NM_020469.3:c.*373A>G	NP_065202.2:n.*373A>G