Canonical Allele Identifier: CA1098940693
Gene:

Linked Data

dbSNP Id: rs1803285993

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17957868del , CM000669.2:g.17957868del GRCh38
NC_000007.13:g.17997491del , CM000669.1:g.17997491del GRCh37
NC_000007.12:g.17964016del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927078.1:n.271-802del