Canonical Allele Identifier: CA375686372

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131684T>C (hg19) ; chr9:g.133256297T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256297T>C , CM000671.2:g.133256297T>C	GRCh38
NC_000009.11:g.136131684T>C , CM000671.1:g.136131684T>C	GRCh37
NC_000009.10:g.135121505T>C	NCBI36
NG_006669.1:g.21371A>G
NG_006669.2:g.23919A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.463A>G
ENST00000647353.1:n.54-5145A>G
ENST00000651471.1:n.389A>G
ENST00000679909.1:c.28+18865A>G	ENSP00000506089.1:n.28+18865A>G
ENST00000453660.3:n.445A>G
ENST00000538324.2:c.431A>G	ENSP00000483018.1:p.His144Arg
ENST00000611156.4:c.431A>G	ENSP00000483265.1:p.His144Arg
NM_020469.2:c.434A>G	NP_065202.2:p.His145Arg
NM_020469.3:c.434A>G	NP_065202.2:p.His145Arg