Canonical Allele Identifier: CA855697467

Gene:

Linked Data

• dbSNP Id: rs1287460087
• MyVariant Identifiers: chr8:g.80103320T>C (hg19) ; chr8:g.79191085T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.79191085T>C , CM000670.2:g.79191085T>C	GRCh38
NC_000008.10:g.80103320T>C , CM000670.1:g.80103320T>C	GRCh37
NC_000008.9:g.80265875T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001745720.1:n.105+714T>C