Canonical Allele Identifier: CA259369475

Gene:

Linked Data

• dbSNP Id: rs1041677424
• gnomAD v3: 14-36384821-A-T
• gnomAD v4: 14-36384821-A-T
• MyVariant Identifiers: chr14:g.36854026A>T (hg19) ; chr14:g.36384821A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.36384821A>T , CM000676.2:g.36384821A>T	GRCh38
NC_000014.8:g.36854026A>T , CM000676.1:g.36854026A>T	GRCh37
NC_000014.7:g.35923777A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011537428.1:c.319-12338A>T	XP_011535730.1:n.319-12338A>T
XR_943756.1:n.358+23725A>T