Canonical Allele Identifier: CA375685295
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255991T>C , CM000671.2:g.133255991T>C GRCh38
NC_000009.11:g.136131378T>C , CM000671.1:g.136131378T>C GRCh37
NC_000009.10:g.135121199T>C NCBI36
NG_006669.1:g.21677A>G
NG_006669.2:g.24225A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.769A>G
ENST00000647353.1:n.54-4839A>G
ENST00000679909.1:c.28+19171A>G ENSP00000506089.1:n.28+19171A>G
ENST00000453660.3:n.751A>G
ENST00000538324.2:c.737A>G ENSP00000483018.1:p.Glu246Gly
ENST00000611156.4:c.737A>G ENSP00000483265.1:p.Glu246Gly
NM_020469.2:c.740A>G NP_065202.2:p.Glu247Gly
NM_020469.3:c.740A>G NP_065202.2:p.Glu247Gly