Canonical Allele Identifier: CA1129724769

Gene: ABO

Linked Data

• dbSNP Id: rs1834958499
• gnomAD v3: 9-133274124-T-A
• gnomAD v4: 9-133274124-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133274124T>A , CM000671.2:g.133274124T>A	GRCh38
NC_000009.11:g.136149540T>A , CM000671.1:g.136149540T>A	GRCh37
NC_000009.10:g.135139361T>A	NCBI36
NG_006669.1:g.3511A>T
NG_006669.2:g.6091A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.58+1038A>T
ENST00000647353.1:n.53+1038A>T
ENST00000651471.1:n.63+1838A>T
ENST00000679909.1:c.28+1038A>T	ENSP00000506089.1:n.28+1038A>T
ENST00000453660.3:n.40+1038A>T
ENST00000538324.2:c.28+1038A>T	ENSP00000483018.1:n.28+1038A>T
ENST00000611156.4:c.28+1038A>T	ENSP00000483265.1:n.28+1038A>T
NM_020469.2:c.28+1038A>T	NP_065202.2:n.28+1038A>T
NM_020469.3:c.28+1038A>T	NP_065202.2:n.28+1038A>T