Canonical Allele Identifier: CA204731033

Gene:

Linked Data

• ClinVar Variation Id: 444139
• ClinVar RCV Id: RCV000626375
• dbSNP Id: rs16923098
• gnomAD v2: 10-23456513-A-C
• gnomAD v3: 10-23167584-A-C
• gnomAD v4: 10-23167584-A-C
• MyVariant Identifiers: chr10:g.23456513A>C (hg19) ; chr10:g.23167584A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.23167584A>C , CM000672.2:g.23167584A>C	GRCh38
NC_000010.10:g.23456513A>C , CM000672.1:g.23456513A>C	GRCh37
NC_000010.9:g.23496519A>C	NCBI36