Canonical Allele Identifier: CA375685218

Gene: ABO

Linked Data

• dbSNP Id: rs1834569710
• MyVariant Identifiers: chr9:g.136131342T>C (hg19) ; chr9:g.133255955T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255955T>C , CM000671.2:g.133255955T>C	GRCh38
NC_000009.11:g.136131342T>C , CM000671.1:g.136131342T>C	GRCh37
NC_000009.10:g.135121163T>C	NCBI36
NG_006669.1:g.21713A>G
NG_006669.2:g.24261A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.805A>G
ENST00000647353.1:n.54-4803A>G
ENST00000679909.1:c.28+19207A>G	ENSP00000506089.1:n.28+19207A>G
ENST00000453660.3:n.787A>G
ENST00000538324.2:c.773A>G	ENSP00000483018.1:p.Asp258Gly
ENST00000611156.4:c.773A>G	ENSP00000483265.1:p.Asp258Gly
NM_020469.2:c.776A>G	NP_065202.2:p.Asp259Gly
NM_020469.3:c.776A>G	NP_065202.2:p.Asp259Gly