Canonical Allele Identifier: CA131177552

Gene:

Linked Data

• dbSNP Id: rs904549118
• MyVariant Identifiers: chr5:g.162083512T>C (hg19) ; chr5:g.162656506T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162656506T>C , CM000667.2:g.162656506T>C	GRCh38
NC_000005.9:g.162083512T>C , CM000667.1:g.162083512T>C	GRCh37
NC_000005.8:g.162016090T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001742958.1:n.418+3596A>G