Canonical Allele Identifier: CA802120342

Gene:

Linked Data

• dbSNP Id: rs1287217630
• MyVariant Identifiers: chr5:g.112996597A>G (hg19) ; chr5:g.113660900A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.113660900A>G , CM000667.2:g.113660900A>G	GRCh38
NC_000005.9:g.112996597A>G , CM000667.1:g.112996597A>G	GRCh37
NC_000005.8:g.113024496A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001742841.1:n.59+27536A>G