Canonical Allele Identifier: CA1899263463
Gene:

Linked Data

dbSNP Id: rs1839589291

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30201668del , CM000672.2:g.30201668del GRCh38
NC_000010.10:g.30490597del , CM000672.1:g.30490597del GRCh37
NC_000010.9:g.30530603del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930791.1:n.1193-1819del
XR_930791.2:n.1449-1819del