Canonical Allele Identifier: CA706741061

Gene:

Linked Data

• dbSNP Id: rs1177430864
• MyVariant Identifiers: chr14:g.52884296G>A (hg19) ; chr14:g.52417578G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.52417578G>A , CM000676.2:g.52417578G>A	GRCh38
NC_000014.8:g.52884296G>A , CM000676.1:g.52884296G>A	GRCh37
NC_000014.7:g.51954046G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_943866.1:n.3125C>T