Canonical Allele Identifier: CA200767706

Gene: ABO

Linked Data

• dbSNP Id: rs587666884
• gnomAD v3: 9-133261756-T-G
• gnomAD v4: 9-133261756-T-G
• MyVariant Identifiers: chr9:g.136137159T>G (hg19) ; chr9:g.133261756T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133261756T>G , CM000671.2:g.133261756T>G	GRCh38
NC_000009.11:g.136137159T>G , CM000671.1:g.136137159T>G	GRCh37
NC_000009.10:g.135126980T>G	NCBI36
NG_006669.1:g.15894A>C
NG_006669.2:g.18459A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.128+343A>C
ENST00000647353.1:n.54-10604A>C
ENST00000651471.1:n.133+343A>C
ENST00000679909.1:c.28+13406A>C	ENSP00000506089.1:n.28+13406A>C
ENST00000453660.3:n.110+343A>C
ENST00000538324.2:c.98+343A>C	ENSP00000483018.1:n.98+343A>C
ENST00000611156.4:c.98+343A>C	ENSP00000483265.1:n.98+343A>C
NM_020469.2:c.98+343A>C	NP_065202.2:n.98+343A>C
NM_020469.3:c.98+343A>C	NP_065202.2:n.98+343A>C