Canonical Allele Identifier: CA561890086

Gene:

Linked Data

• ClinVar Variation Id: 469887
• ClinVar RCV Id: RCV003767024
• dbSNP Id: rs1192399402
• gnomAD v2: 5-112043082-G-C
• gnomAD v3: 5-112707385-G-C
• gnomAD v4: 5-112707385-G-C
• MyVariant Identifiers: chr5:g.112043082G>C (hg19) ; chr5:g.112707385G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707385G>C , CM000667.2:g.112707385G>C	GRCh38
NC_000005.9:g.112043082G>C , CM000667.1:g.112043082G>C	GRCh37
NC_000005.8:g.112070981G>C	NCBI36
NG_008481.4:g.19865G>C , LRG_130:g.19865G>C