Canonical Allele Identifier: CA202788800
Gene:

Linked Data

dbSNP Id: rs756117994

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8697687del , CM000672.2:g.8697687del GRCh38
NC_000010.10:g.8739650del , CM000672.1:g.8739650del GRCh37
NC_000010.9:g.8779656del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930641.1:n.33-27886del