Canonical Allele Identifier: CA1630848044
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257246A= , CM000671.2:g.133257246A= GRCh38
NC_000009.11:g.136132633A= , CM000671.1:g.136132633A= GRCh37
NC_000009.10:g.135122454A= NCBI36
NG_006669.1:g.20422T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.403+163T=
ENST00000647353.1:n.54-6094T=
ENST00000651471.1:n.329+796T=
ENST00000679909.1:c.28+17916T= ENSP00000506089.1:n.28+17916T=
ENST00000453660.3:n.385+163T=
ENST00000538324.2:c.371+163T= ENSP00000483018.1:n.371+163T=
ENST00000611156.4:c.371+163T= ENSP00000483265.1:n.371+163T=
NM_020469.2:c.374+163T= NP_065202.2:n.374+163T=
NM_020469.3:c.374+163T= NP_065202.2:n.374+163T=