Canonical Allele Identifier: CA261374891

Gene:

Linked Data

• dbSNP Id: rs891921590
• gnomAD v2: 14-52884408-C-A
• gnomAD v3: 14-52417690-C-A
• gnomAD v4: 14-52417690-C-A
• MyVariant Identifiers: chr14:g.52884408C>A (hg19) ; chr14:g.52417690C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.52417690C>A , CM000676.2:g.52417690C>A	GRCh38
NC_000014.8:g.52884408C>A , CM000676.1:g.52884408C>A	GRCh37
NC_000014.7:g.51954158C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_943866.1:n.3013G>T