Canonical Allele Identifier: CA658655872

Gene:

Linked Data

• ClinVar Variation Id: 469886
• ClinVar RCV Id: RCV003651965
• dbSNP Id: rs1351477360
• gnomAD v4: 5-112707386-G-C
• MyVariant Identifiers: chr5:g.112043083G>C (hg19) ; chr5:g.112707386G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707386G>C , CM000667.2:g.112707386G>C	GRCh38
NC_000005.9:g.112043083G>C , CM000667.1:g.112043083G>C	GRCh37
NC_000005.8:g.112070982G>C	NCBI36
NG_008481.4:g.19866G>C , LRG_130:g.19866G>C