Canonical Allele Identifier: CA375686297

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131651G>C (hg19) ; chr9:g.133256264G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256264G>C , CM000671.2:g.133256264G>C	GRCh38
NC_000009.11:g.136131651G>C , CM000671.1:g.136131651G>C	GRCh37
NC_000009.10:g.135121472G>C	NCBI36
NG_006669.1:g.21404C>G
NG_006669.2:g.23952C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.496C>G
ENST00000647353.1:n.54-5112C>G
ENST00000651471.1:n.422C>G
ENST00000679909.1:c.28+18898C>G	ENSP00000506089.1:n.28+18898C>G
ENST00000453660.3:n.478C>G
ENST00000538324.2:c.464C>G	ENSP00000483018.1:p.Pro155Arg
ENST00000611156.4:c.464C>G	ENSP00000483265.1:p.Pro155Arg
NM_020469.2:c.467C>G	NP_065202.2:p.Pro156Arg
NM_020469.3:c.467C>G	NP_065202.2:p.Pro156Arg