Canonical Allele Identifier: CA259369471

Gene:

Linked Data

• dbSNP Id: rs893044760
• MyVariant Identifiers: chr14:g.36853982G>A (hg19) ; chr14:g.36384777G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.36384777G>A , CM000676.2:g.36384777G>A	GRCh38
NC_000014.8:g.36853982G>A , CM000676.1:g.36853982G>A	GRCh37
NC_000014.7:g.35923733G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011537428.1:c.319-12382G>A	XP_011535730.1:n.319-12382G>A
XR_943756.1:n.358+23681G>A