Canonical Allele Identifier: CA13337234

Gene:

Linked Data

• ClinVar Variation Id: 1247676
• ClinVar RCV Id: RCV001649637
• dbSNP Id: rs2486758
• gnomAD v2: 10-104597480-T-C
• gnomAD v3: 10-102837723-T-C
• gnomAD v4: 10-102837723-T-C
• MyVariant Identifiers: chr10:g.104597480T>C (hg19) ; chr10:g.102837723T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102837723T>C , CM000672.2:g.102837723T>C	GRCh38
NC_000010.10:g.104597480T>C , CM000672.1:g.104597480T>C	GRCh37
NC_000010.9:g.104587470T>C	NCBI36
NG_007955.1:g.4811A>G