Canonical Allele Identifier: CA1882579751
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255881A= , CM000671.2:g.133255881A= GRCh38
NC_000009.11:g.136131268A= , CM000671.1:g.136131268A= GRCh37
NC_000009.10:g.135121089A= NCBI36
NG_006669.1:g.21787T=
NG_006669.2:g.24335T=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.879T=
ENST00000647353.1:n.54-4729T=
ENST00000679909.1:c.28+19281T= ENSP00000506089.1:n.28+19281T=
ENST00000453660.3:n.861T=
ENST00000538324.2:c.847T= ENSP00000483018.1:p.Cys283=
ENST00000611156.4:c.847T= ENSP00000483265.1:p.Cys283=
NM_020469.2:c.850T= NP_065202.2:p.Cys284=
NM_020469.3:c.850T= NP_065202.2:p.Cys284=