Canonical Allele Identifier: CA1882583129
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258131T= , CM000671.2:g.133258131T= GRCh38
NC_000009.11:g.136133521T= , CM000671.1:g.136133521T= GRCh37
NC_000009.10:g.135123342T= NCBI36
NG_006669.1:g.19533A=
NG_006669.2:g.22084A=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.235A=
ENST00000647353.1:n.54-6979A=
ENST00000651471.1:n.240A=
ENST00000679909.1:c.28+17031A= ENSP00000506089.1:n.28+17031A=
ENST00000453660.3:n.217A=
ENST00000538324.2:c.205A= ENSP00000483018.1:p.Met69=
ENST00000611156.4:c.205A= ENSP00000483265.1:p.Met69=
NM_020469.2:c.205A= NP_065202.2:p.Met69=
NM_020469.3:c.205A= NP_065202.2:p.Met69=