Canonical Allele Identifier: CA658843446

Gene:

Linked Data

• dbSNP Id: rs550113879
• gnomAD v3: 10-100101786-T-A
• gnomAD v4: 10-100101786-T-A
• MyVariant Identifiers: chr10:g.101861543T>A (hg19) ; chr10:g.100101786T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100101786T>A , CM000672.2:g.100101786T>A	GRCh38
NC_000010.10:g.101861543T>A , CM000672.1:g.101861543T>A	GRCh37
NC_000010.9:g.101851533T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_946245.1:n.185+5549T>A