Canonical Allele Identifier: CA1083723782
Gene:

Linked Data

dbSNP Id: rs1756515815

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162656593del , CM000667.2:g.162656593del GRCh38
NC_000005.9:g.162083599del , CM000667.1:g.162083599del GRCh37
NC_000005.8:g.162016177del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742958.1:n.418+3509del