Canonical Allele Identifier: CA779336896
Gene:

Linked Data

dbSNP Id: rs1172166589

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.41477596del , CM000680.2:g.41477596del GRCh38
NC_000018.9:g.39057560del , CM000680.1:g.39057560del GRCh37
NC_000018.8:g.37311558del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935409.1:n.86-26538del