Canonical Allele Identifier: CA806711260

Gene:

Linked Data

• dbSNP Id: rs1211918736
• MyVariant Identifiers: chr5:g.162083546C>T (hg19) ; chr5:g.162656540C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162656540C>T , CM000667.2:g.162656540C>T	GRCh38
NC_000005.9:g.162083546C>T , CM000667.1:g.162083546C>T	GRCh37
NC_000005.8:g.162016124C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001742958.1:n.418+3562G>A