Canonical Allele Identifier: CA779336964

Gene:

Linked Data

• dbSNP Id: rs1404541206
• MyVariant Identifiers: chr18:g.39057701C>G (hg19) ; chr18:g.41477737C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.41477737C>G , CM000680.2:g.41477737C>G	GRCh38
NC_000018.9:g.39057701C>G , CM000680.1:g.39057701C>G	GRCh37
NC_000018.8:g.37311699C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935409.1:n.86-26397C>G