Canonical Allele Identifier: CA299344137

Gene:

Linked Data

• dbSNP Id: rs986684334
• MyVariant Identifiers: chr18:g.41477799G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.41477799G>T , CM000680.2:g.41477799G>T	GRCh38
NC_000018.9:g.39057763G>T , CM000680.1:g.39057763G>T	GRCh37
NC_000018.8:g.37311761G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_935409.1:n.86-26335G>T