Canonical Allele Identifier: CA833583382

Gene:

Linked Data

• dbSNP Id: rs889161098
• MyVariant Identifiers: chr7:g.13440181T>C (hg19) ; chr7:g.13400556T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.13400556T>C , CM000669.2:g.13400556T>C	GRCh38
NC_000007.13:g.13440181T>C , CM000669.1:g.13440181T>C	GRCh37
NC_000007.12:g.13406706T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001745097.1:n.147+90233T>C