Canonical Allele Identifier: CA2700015851
Gene:

Linked Data

dbSNP Id: rs2104588016

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016106_88016107del , CM000664.2:g.88016106_88016107del GRCh38
NC_000002.11:g.88315625_88315626del , CM000664.1:g.88315625_88315626del GRCh37
NC_000002.10:g.88096740_88096741del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.451_452del
XR_940336.3:n.451_452del