Canonical Allele Identifier: CA2954282204
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257330del , CM000671.2:g.133257330del GRCh38
NC_000009.11:g.136132717del , CM000671.1:g.136132717del GRCh37
NC_000009.10:g.135122538del NCBI36
NG_006669.1:g.20338del
NG_006669.2:g.22886del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.403+79del
ENST00000647353.1:n.54-6178del
ENST00000651471.1:n.329+712del
ENST00000679909.1:c.28+17832del ENSP00000506089.1:n.28+17832del
ENST00000453660.3:n.385+79del
ENST00000538324.2:c.371+79del ENSP00000483018.1:n.371+79del
ENST00000611156.4:c.371+79del ENSP00000483265.1:n.371+79del
NM_020469.2:c.374+79del NP_065202.2:n.374+79del
NM_020469.3:c.374+79del NP_065202.2:n.374+79del