Canonical Allele Identifier: CA553749099
Gene:

Linked Data

dbSNP Id: rs1335448163

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499869del , CM000666.2:g.102499869del GRCh38
NC_000004.11:g.103421026del , CM000666.1:g.103421026del GRCh37
NC_000004.10:g.103640058del NCBI36
NG_050628.1:g.3541del

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1380del XP_011530769.1:n.643+1380del
NR_136202.1:n.48+2570del