Canonical Allele Identifier: CA917964998

Gene:

Linked Data

• dbSNP Id: rs1562798191

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24283344del , CM000669.2:g.24283344del	GRCh38
NC_000007.13:g.24322963del , CM000669.1:g.24322963del	GRCh37
NC_000007.12:g.24289488del	NCBI36
NG_016148.1:g.4157del

Transcript Alleles

HGVS	Amino-acid Change
XM_017012910.1:c.42-27640del	XP_016868399.1:n.42-27640del
XM_017012911.1:c.42-27640del	XP_016868400.1:n.42-27640del
XR_001745121.1:n.473+36018del
XR_001745122.1:n.345-86310del
XR_001745123.1:n.473+36018del
XR_001745124.1:n.473+36018del
XR_001745125.1:n.473+36018del
XR_001745126.1:n.473+36018del
XR_001745127.1:n.345-27640del
XR_001745129.1:n.473+36018del
XR_001745130.1:n.473+36018del
XR_001745131.1:n.473+36018del
XR_001745132.1:n.473+36018del