Canonical Allele Identifier: CA1129714844
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255451del , CM000671.2:g.133255451del GRCh38
NC_000009.11:g.136130838del , CM000671.1:g.136130838del GRCh37
NC_000009.10:g.135120659del NCBI36
NG_006669.1:g.22220del
NG_006669.2:g.24768del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1312del
ENST00000647353.1:n.54-4296del
ENST00000679909.1:c.28+19714del ENSP00000506089.1:n.28+19714del
ENST00000453660.3:n.1294del
ENST00000611156.4:c.*218del ENSP00000483265.1:n.*218del
NM_020469.2:c.*218del NP_065202.2:n.*218del
NM_020469.3:c.*218del NP_065202.2:n.*218del