Canonical Allele Identifier: CA212877285

Gene:

Linked Data

• dbSNP Id: rs559861988
• gnomAD v3: 10-100101680-C-T
• gnomAD v4: 10-100101680-C-T
• MyVariant Identifiers: chr10:g.101861437C>T (hg19) ; chr10:g.100101680C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100101680C>T , CM000672.2:g.100101680C>T	GRCh38
NC_000010.10:g.101861437C>T , CM000672.1:g.101861437C>T	GRCh37
NC_000010.9:g.101851427C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_946245.1:n.185+5443C>T