Canonical Allele Identifier: CA124924667

Gene:

Linked Data

• ClinVar Variation Id: 645275
• ClinVar RCV Id: RCV003535904
• dbSNP Id: rs968227350
• gnomAD v4: 5-112707440-C-A
• MyVariant Identifiers: chr5:g.112043137C>A (hg19) ; chr5:g.112707440C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707440C>A , CM000667.2:g.112707440C>A	GRCh38
NC_000005.9:g.112043137C>A , CM000667.1:g.112043137C>A	GRCh37
NC_000005.8:g.112071036C>A	NCBI36
NG_008481.4:g.19920C>A , LRG_130:g.19920C>A