Canonical Allele Identifier: CA658843382

Gene:

Linked Data

• dbSNP Id: rs1325479810
• MyVariant Identifiers: chr10:g.101861455T>C (hg19) ; chr10:g.100101698T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100101698T>C , CM000672.2:g.100101698T>C	GRCh38
NC_000010.10:g.101861455T>C , CM000672.1:g.101861455T>C	GRCh37
NC_000010.9:g.101851445T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_946245.1:n.185+5461T>C