Canonical Allele Identifier: CA299344127

Gene:

Linked Data

• dbSNP Id: rs762054870
• MyVariant Identifiers: chr18:g.39057648A>G (hg19) ; chr18:g.41477684A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.41477684A>G , CM000680.2:g.41477684A>G	GRCh38
NC_000018.9:g.39057648A>G , CM000680.1:g.39057648A>G	GRCh37
NC_000018.8:g.37311646A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935409.1:n.86-26450A>G