Canonical Allele Identifier: CA212877293

Gene:

Linked Data

• dbSNP Id: rs546016201
• gnomAD v3: 10-100101701-A-G
• gnomAD v4: 10-100101701-A-G
• MyVariant Identifiers: chr10:g.101861458A>G (hg19) ; chr10:g.100101701A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100101701A>G , CM000672.2:g.100101701A>G	GRCh38
NC_000010.10:g.101861458A>G , CM000672.1:g.101861458A>G	GRCh37
NC_000010.9:g.101851448A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_946245.1:n.185+5464A>G