Canonical Allele Identifier: CA779336968

Gene:

Linked Data

• dbSNP Id: rs2848745
• MyVariant Identifiers: chr18:g.39057725G>A (hg19) ; chr18:g.41477761G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.41477761G>A , CM000680.2:g.41477761G>A	GRCh38
NC_000018.9:g.39057725G>A , CM000680.1:g.39057725G>A	GRCh37
NC_000018.8:g.37311723G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_935409.1:n.86-26373G>A