Canonical Allele Identifier: CA202788783
Gene:

Linked Data

dbSNP Id: rs965465989

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8697547del , CM000672.2:g.8697547del GRCh38
NC_000010.10:g.8739510del , CM000672.1:g.8739510del GRCh37
NC_000010.9:g.8779516del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930641.1:n.33-27743del