Canonical Allele Identifier: CA2954282208
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257332del , CM000671.2:g.133257332del GRCh38
NC_000009.11:g.136132719del , CM000671.1:g.136132719del GRCh37
NC_000009.10:g.135122540del NCBI36
NG_006669.1:g.20337del
NG_006669.2:g.22885del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.403+78del
ENST00000647353.1:n.54-6179del
ENST00000651471.1:n.329+711del
ENST00000679909.1:c.28+17831del ENSP00000506089.1:n.28+17831del
ENST00000453660.3:n.385+78del
ENST00000538324.2:c.371+78del ENSP00000483018.1:n.371+78del
ENST00000611156.4:c.371+78del ENSP00000483265.1:n.371+78del
NM_020469.2:c.374+78del NP_065202.2:n.374+78del
NM_020469.3:c.374+78del NP_065202.2:n.374+78del