Canonical Allele Identifier: CA1882582622
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257678G= , CM000671.2:g.133257678G= GRCh38
NC_000009.11:g.136133065G= , CM000671.1:g.136133065G= GRCh37
NC_000009.10:g.135122886G= NCBI36
NG_006669.1:g.19989C=
NG_006669.2:g.22537C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.270-136C=
ENST00000647353.1:n.54-6526C=
ENST00000651471.1:n.329+364C=
ENST00000679909.1:c.28+17484C= ENSP00000506089.1:n.28+17484C=
ENST00000453660.3:n.252-136C=
ENST00000538324.2:c.240-136C= ENSP00000483018.1:n.240-136C=
ENST00000611156.4:c.240-136C= ENSP00000483265.1:n.240-136C=
NM_020469.2:c.240-136C= NP_065202.2:n.240-136C=
NM_020469.3:c.240-136C= NP_065202.2:n.240-136C=