Canonical Allele Identifier: CA838530798

Gene:

Linked Data

• dbSNP Id: rs1323975966
• MyVariant Identifiers: chr7:g.41821930G>C (hg19) ; chr7:g.41782332G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.41782332G>C , CM000669.2:g.41782332G>C	GRCh38
NC_000007.13:g.41821930G>C , CM000669.1:g.41821930G>C	GRCh37
NC_000007.12:g.41788455G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001745185.1:n.964+46618G>C
XR_001745186.1:n.954+46628G>C