Canonical Allele Identifier: CA259369488

Gene:

Linked Data

• dbSNP Id: rs866496522
• MyVariant Identifiers: chr14:g.36854147G>T (hg19) ; chr14:g.36384942G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.36384942G>T , CM000676.2:g.36384942G>T	GRCh38
NC_000014.8:g.36854147G>T , CM000676.1:g.36854147G>T	GRCh37
NC_000014.7:g.35923898G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011537428.1:c.319-12217G>T	XP_011535730.1:n.319-12217G>T
XR_943756.1:n.358+23846G>T