Canonical Allele Identifier: CA705306391

Gene:

Linked Data

• dbSNP Id: rs1257800779
• MyVariant Identifiers: chr14:g.36854162T>G (hg19) ; chr14:g.36384957T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.36384957T>G , CM000676.2:g.36384957T>G	GRCh38
NC_000014.8:g.36854162T>G , CM000676.1:g.36854162T>G	GRCh37
NC_000014.7:g.35923913T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011537428.1:c.319-12202T>G	XP_011535730.1:n.319-12202T>G
XR_943756.1:n.358+23861T>G