Canonical Allele Identifier: CA1882579055
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255608C= , CM000671.2:g.133255608C= GRCh38
NC_000009.11:g.136130995C= , CM000671.1:g.136130995C= GRCh37
NC_000009.10:g.135120816C= NCBI36
NG_006669.1:g.22060G=
NG_006669.2:g.24608G=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.1152G=
ENST00000647353.1:n.54-4456G=
ENST00000679909.1:c.28+19554G= ENSP00000506089.1:n.28+19554G=
ENST00000453660.3:n.1134G=
ENST00000538324.2:c.1116G= ENSP00000483018.1:p.Trp372=
ENST00000611156.4:c.*58G= ENSP00000483265.1:n.*58G=
NM_020469.2:c.*58G= NP_065202.2:n.*58G=
NM_020469.3:c.*58G= NP_065202.2:n.*58G=