Canonical Allele Identifier: CA202098452

Gene:

Linked Data

• dbSNP Id: rs950756507
• gnomAD v2: 10-4151149-T-C
• gnomAD v3: 10-4108957-T-C
• gnomAD v4: 10-4108957-T-C
• MyVariant Identifiers: chr10:g.4151149T>C (hg19) ; chr10:g.4108957T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.4108957T>C , CM000672.2:g.4108957T>C	GRCh38
NC_000010.10:g.4151149T>C , CM000672.1:g.4151149T>C	GRCh37
NC_000010.9:g.4141149T>C	NCBI36