Canonical Allele Identifier: CA658796598

Gene:

Linked Data

• ClinVar Variation Id: 537640
• ClinVar RCV Id: RCV003538570
• dbSNP Id: rs1280021363
• gnomAD v4: 5-112707454-T-C
• MyVariant Identifiers: chr5:g.112043151T>C (hg19) ; chr5:g.112707454T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707454T>C , CM000667.2:g.112707454T>C	GRCh38
NC_000005.9:g.112043151T>C , CM000667.1:g.112043151T>C	GRCh37
NC_000005.8:g.112071050T>C	NCBI36
NG_008481.4:g.19934T>C , LRG_130:g.19934T>C