Canonical Allele Identifier: CA10654419

Gene:

Linked Data

• ClinVar Variation Id: 368794
• ClinVar RCV Id: RCV000289173 ; RCV000343588 ; RCV000394684
• dbSNP Id: rs3748581
• gnomAD v2: 1-10441664-T-C
• gnomAD v3: 1-10381606-T-C
• gnomAD v4: 1-10381606-T-C
• MyVariant Identifiers: chr1:g.10441664T>C (hg19) ; chr1:g.10381606T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.10381606T>C , CM000663.2:g.10381606T>C	GRCh38
NC_000001.10:g.10441664T>C , CM000663.1:g.10441664T>C	GRCh37
NC_000001.9:g.10364251T>C	NCBI36
NG_008069.1:g.175901T>C , LRG_252:g.175901T>C