Canonical Allele Identifier: CA202788782

Gene:

Linked Data

• dbSNP Id: rs899313139
• MyVariant Identifiers: chr10:g.8739499G>A (hg19) ; chr10:g.8697536G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.8697536G>A , CM000672.2:g.8697536G>A	GRCh38
NC_000010.10:g.8739499G>A , CM000672.1:g.8739499G>A	GRCh37
NC_000010.9:g.8779505G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930641.1:n.33-27735C>T