Canonical Allele Identifier: CA1882580933
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256315T= , CM000671.2:g.133256315T= GRCh38
NC_000009.11:g.136131702T= , CM000671.1:g.136131702T= GRCh37
NC_000009.10:g.135121523T= NCBI36
NG_006669.1:g.21353A=
NG_006669.2:g.23901A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.445A=
ENST00000647353.1:n.54-5163A=
ENST00000651471.1:n.371A=
ENST00000679909.1:c.28+18847A= ENSP00000506089.1:n.28+18847A=
ENST00000453660.3:n.427A=
ENST00000538324.2:c.413A= ENSP00000483018.1:p.Lys138=
ENST00000611156.4:c.413A= ENSP00000483265.1:p.Lys138=
NM_020469.2:c.416A= NP_065202.2:p.Lys139=
NM_020469.3:c.416A= NP_065202.2:p.Lys139=