Canonical Allele Identifier: CA780108977

Gene:

Linked Data

• dbSNP Id: rs1294225099
• MyVariant Identifiers: chr18:g.47172310C>T (hg19) ; chr18:g.49645940C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.49645940C>T , CM000680.2:g.49645940C>T	GRCh38
NC_000018.9:g.47172310C>T , CM000680.1:g.47172310C>T	GRCh37
NC_000018.8:g.45426308C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935461.1:n.162-16094C>T
XR_001753446.1:n.898-16094C>T