Canonical Allele Identifier: CA131177563

Gene:

Linked Data

• dbSNP Id: rs1005896221
• MyVariant Identifiers: chr5:g.162083591T>A (hg19) ; chr5:g.162656585T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162656585T>A , CM000667.2:g.162656585T>A	GRCh38
NC_000005.9:g.162083591T>A , CM000667.1:g.162083591T>A	GRCh37
NC_000005.8:g.162016169T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001742958.1:n.418+3517A>T