Canonical Allele Identifier: CA265581616

Gene:

Linked Data

• dbSNP Id: rs1033969904
• MyVariant Identifiers: chr14:g.92781008A>G (hg19) ; chr14:g.92314664A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92314664A>G , CM000676.2:g.92314664A>G	GRCh38
NC_000014.8:g.92781008A>G , CM000676.1:g.92781008A>G	GRCh37
NC_000014.7:g.91850761A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_944153.1:n.132-582A>G