Canonical Allele Identifier: CA1882590667
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133274357T= , CM000671.2:g.133274357T= GRCh38
NC_000009.11:g.136149773T= , CM000671.1:g.136149773T= GRCh37
NC_000009.10:g.135139594T= NCBI36
NG_006669.1:g.3277A=
NG_006669.2:g.5858A=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.58+805A=
ENST00000647353.1:n.53+805A=
ENST00000651471.1:n.63+1605A=
ENST00000679909.1:c.28+805A= ENSP00000506089.1:n.28+805A=
ENST00000453660.3:n.40+805A=
ENST00000538324.2:c.28+805A= ENSP00000483018.1:n.28+805A=
ENST00000611156.4:c.28+805A= ENSP00000483265.1:n.28+805A=
NM_020469.2:c.28+805A= NP_065202.2:n.28+805A=
NM_020469.3:c.28+805A= NP_065202.2:n.28+805A=