Canonical Allele Identifier: CA833583316

Gene:

Linked Data

• dbSNP Id: rs1359172009
• MyVariant Identifiers: chr7:g.13440156T>C (hg19) ; chr7:g.13400531T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.13400531T>C , CM000669.2:g.13400531T>C	GRCh38
NC_000007.13:g.13440156T>C , CM000669.1:g.13440156T>C	GRCh37
NC_000007.12:g.13406681T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001745097.1:n.147+90208T>C