Canonical Allele Identifier: CA375684880

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131286G>T (hg19) ; chr9:g.133255899G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255899G>T , CM000671.2:g.133255899G>T	GRCh38
NC_000009.11:g.136131286G>T , CM000671.1:g.136131286G>T	GRCh37
NC_000009.10:g.135121107G>T	NCBI36
NG_006669.1:g.21769C>A
NG_006669.2:g.24317C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.861C>A
ENST00000647353.1:n.54-4747C>A
ENST00000679909.1:c.28+19263C>A	ENSP00000506089.1:n.28+19263C>A
ENST00000453660.3:n.843C>A
ENST00000538324.2:c.829C>A	ENSP00000483018.1:p.Gln277Lys
ENST00000611156.4:c.829C>A	ENSP00000483265.1:p.Gln277Lys
NM_020469.2:c.832C>A	NP_065202.2:p.Gln278Lys
NM_020469.3:c.832C>A	NP_065202.2:p.Gln278Lys