Canonical Allele Identifier: CA705306413

Gene:

Linked Data

• dbSNP Id: rs1319442408
• gnomAD v3: 14-36385029-T-A
• gnomAD v4: 14-36385029-T-A
• MyVariant Identifiers: chr14:g.36854234T>A (hg19) ; chr14:g.36385029T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.36385029T>A , CM000676.2:g.36385029T>A	GRCh38
NC_000014.8:g.36854234T>A , CM000676.1:g.36854234T>A	GRCh37
NC_000014.7:g.35923985T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011537428.1:c.319-12130T>A	XP_011535730.1:n.319-12130T>A
XR_943756.1:n.358+23933T>A