Canonical Allele Identifier: CA1882580286
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256078T= , CM000671.2:g.133256078T= GRCh38
NC_000009.11:g.136131465T= , CM000671.1:g.136131465T= GRCh37
NC_000009.10:g.135121286T= NCBI36
NG_006669.1:g.21590A=
NG_006669.2:g.24138A=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.682A=
ENST00000647353.1:n.54-4926A=
ENST00000679909.1:c.28+19084A= ENSP00000506089.1:n.28+19084A=
ENST00000453660.3:n.664A=
ENST00000538324.2:c.650A= ENSP00000483018.1:p.Asp217=
ENST00000611156.4:c.650A= ENSP00000483265.1:p.Asp217=
NM_020469.2:c.653A= NP_065202.2:p.Asp218=
NM_020469.3:c.653A= NP_065202.2:p.Asp218=