Canonical Allele Identifier: CA205533607

Gene:

Linked Data

• dbSNP Id: rs542466467
• gnomAD v3: 10-30201848-C-G
• gnomAD v4: 10-30201848-C-G
• MyVariant Identifiers: chr10:g.30490777C>G (hg19) ; chr10:g.30201848C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.30201848C>G , CM000672.2:g.30201848C>G	GRCh38
NC_000010.10:g.30490777C>G , CM000672.1:g.30490777C>G	GRCh37
NC_000010.9:g.30530783C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930791.1:n.1193-1639C>G
XR_930791.2:n.1449-1639C>G