Canonical Allele Identifier: CA259369481

Gene:

Linked Data

• dbSNP Id: rs941320713
• gnomAD v3: 14-36384883-C-T
• gnomAD v4: 14-36384883-C-T
• MyVariant Identifiers: chr14:g.36854088C>T (hg19) ; chr14:g.36384883C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.36384883C>T , CM000676.2:g.36384883C>T	GRCh38
NC_000014.8:g.36854088C>T , CM000676.1:g.36854088C>T	GRCh37
NC_000014.7:g.35923839C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011537428.1:c.319-12276C>T	XP_011535730.1:n.319-12276C>T
XR_943756.1:n.358+23787C>T