Canonical Allele Identifier: CA10654506

Gene:

Linked Data

• ClinVar Variation Id: 369056
• ClinVar RCV Id: RCV000287930 ; RCV000329077 ; RCV000352241 ; RCV000382316 ; RCV000398293
• dbSNP Id: rs11839674
• gnomAD v2: 13-20761593-C-T
• gnomAD v3: 13-20187454-C-T
• gnomAD v4: 13-20187454-C-T
• MyVariant Identifiers: chr13:g.20761593C>T (hg19) ; chr13:g.20187454C>T (hg38)
• PubMed: PMID:22567369

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.20187454C>T , CM000675.2:g.20187454C>T	GRCh38
NC_000013.10:g.20761593C>T , CM000675.1:g.20761593C>T	GRCh37
NC_000013.9:g.19659593C>T	NCBI36
NG_008358.1:g.10522G>A