Canonical Allele Identifier: CA778454379

Gene:

Linked Data

• dbSNP Id: rs1381738973
• MyVariant Identifiers: chr18:g.29337002T>A (hg19) ; chr18:g.31757039T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31757039T>A , CM000680.2:g.31757039T>A	GRCh38
NC_000018.9:g.29337002T>A , CM000680.1:g.29337002T>A	GRCh37
NC_000018.8:g.27591000T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935338.1:n.66-5100T>A