Canonical Allele Identifier: CA1033291884
Gene:

Linked Data

dbSNP Id: rs1656297695

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016413del , CM000664.2:g.88016413del GRCh38
NC_000002.11:g.88315932del , CM000664.1:g.88315932del GRCh37
NC_000002.10:g.88097047del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.758del
XR_940336.3:n.758del