Canonical Allele Identifier: CA261374877

Gene:

Linked Data

• dbSNP Id: rs975906736
• MyVariant Identifiers: chr14:g.52884283A>G (hg19) ; chr14:g.52417565A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.52417565A>G , CM000676.2:g.52417565A>G	GRCh38
NC_000014.8:g.52884283A>G , CM000676.1:g.52884283A>G	GRCh37
NC_000014.7:g.51954033A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_943866.1:n.3138T>C