Canonical Allele Identifier: CA562115668
Gene:

Linked Data

dbSNP Id: rs1262347732

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113660910del , CM000667.2:g.113660910del GRCh38
NC_000005.9:g.112996607del , CM000667.1:g.112996607del GRCh37
NC_000005.8:g.113024506del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001742841.1:n.59+27546del