Canonical Allele Identifier: CA1882579772
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255893G= , CM000671.2:g.133255893G= GRCh38
NC_000009.11:g.136131280G= , CM000671.1:g.136131280G= GRCh37
NC_000009.10:g.135121101G= NCBI36
NG_006669.1:g.21775C=
NG_006669.2:g.24323C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.867C=
ENST00000647353.1:n.54-4741C=
ENST00000679909.1:c.28+19269C= ENSP00000506089.1:n.28+19269C=
ENST00000453660.3:n.849C=
ENST00000538324.2:c.835C= ENSP00000483018.1:p.Leu279=
ENST00000611156.4:c.835C= ENSP00000483265.1:p.Leu279=
NM_020469.2:c.838C= NP_065202.2:p.Leu280=
NM_020469.3:c.838C= NP_065202.2:p.Leu280=