Canonical Allele Identifier: CA1882580097
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255997G= , CM000671.2:g.133255997G= GRCh38
NC_000009.11:g.136131384G= , CM000671.1:g.136131384G= GRCh37
NC_000009.10:g.135121205G= NCBI36
NG_006669.1:g.21671C=
NG_006669.2:g.24219C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.763C=
ENST00000647353.1:n.54-4845C=
ENST00000679909.1:c.28+19165C= ENSP00000506089.1:n.28+19165C=
ENST00000453660.3:n.745C=
ENST00000538324.2:c.731C= ENSP00000483018.1:p.Thr244=
ENST00000611156.4:c.731C= ENSP00000483265.1:p.Thr244=
NM_020469.2:c.734C= NP_065202.2:p.Thr245=
NM_020469.3:c.734C= NP_065202.2:p.Thr245=