Canonical Allele Identifier: CA2579497364
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257319del , CM000671.2:g.133257319del GRCh38
NC_000009.11:g.136132706del , CM000671.1:g.136132706del GRCh37
NC_000009.10:g.135122527del NCBI36
NG_006669.1:g.20352del
NG_006669.2:g.22900del

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+93del
ENST00000647353.1:n.54-6164del
ENST00000651471.1:n.329+726del
ENST00000679909.1:c.28+17846del ENSP00000506089.1:n.28+17846del
ENST00000453660.3:n.385+93del
ENST00000538324.2:c.371+93del ENSP00000483018.1:n.371+93del
ENST00000611156.4:c.371+93del ENSP00000483265.1:n.371+93del
NM_020469.2:c.374+93del NP_065202.2:n.374+93del
NM_020469.3:c.374+93del NP_065202.2:n.374+93del