Canonical Allele Identifier: CA1882578534
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255368G= , CM000671.2:g.133255368G= GRCh38
NC_000009.11:g.136130755G= , CM000671.1:g.136130755G= GRCh37
NC_000009.10:g.135120576G= NCBI36
NG_006669.1:g.22300C=
NG_006669.2:g.24848C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1392C=
ENST00000647353.1:n.54-4216C=
ENST00000679909.1:c.28+19794C= ENSP00000506089.1:n.28+19794C=
ENST00000453660.3:n.1374C=
ENST00000611156.4:c.*298C= ENSP00000483265.1:n.*298C=
NM_020469.2:c.*298C= NP_065202.2:n.*298C=
NM_020469.3:c.*298C= NP_065202.2:n.*298C=