Canonical Allele Identifier: CA1882579957
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255943A= , CM000671.2:g.133255943A= GRCh38
NC_000009.11:g.136131330A= , CM000671.1:g.136131330A= GRCh37
NC_000009.10:g.135121151A= NCBI36
NG_006669.1:g.21725T=
NG_006669.2:g.24273T=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.817T=
ENST00000647353.1:n.54-4791T=
ENST00000679909.1:c.28+19219T= ENSP00000506089.1:n.28+19219T=
ENST00000453660.3:n.799T=
ENST00000538324.2:c.785T= ENSP00000483018.1:p.Phe262=
ENST00000611156.4:c.785T= ENSP00000483265.1:p.Phe262=
NM_020469.2:c.788T= NP_065202.2:p.Phe263=
NM_020469.3:c.788T= NP_065202.2:p.Phe263=