Canonical Allele Identifier: CA806711257

Gene:

Linked Data

• dbSNP Id: rs1181354130
• MyVariant Identifiers: chr5:g.162083545del (hg19) ; chr5:g.162656539del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162656541del , CM000667.2:g.162656541del	GRCh38
NC_000005.9:g.162083547del , CM000667.1:g.162083547del	GRCh37
NC_000005.8:g.162016125del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001742958.1:n.418+3563del