Canonical Allele Identifier: CA591611645

Gene:

Linked Data

• dbSNP Id: rs1369634240
• gnomAD v2: 10-4151123-C-T
• MyVariant Identifiers: chr10:g.4151123C>T (hg19) ; chr10:g.4108931C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.4108931C>T , CM000672.2:g.4108931C>T	GRCh38
NC_000010.10:g.4151123C>T , CM000672.1:g.4151123C>T	GRCh37
NC_000010.9:g.4141123C>T	NCBI36