Canonical Allele Identifier: CA124924533

Gene:

Linked Data

• ClinVar Variation Id: 469902
• ClinVar RCV Id: RCV003537063
• dbSNP Id: rs931897682
• gnomAD v3: 5-112707318-C-G
• gnomAD v4: 5-112707318-C-G
• MyVariant Identifiers: chr5:g.112043015C>G (hg19) ; chr5:g.112707318C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707318C>G , CM000667.2:g.112707318C>G	GRCh38
NC_000005.9:g.112043015C>G , CM000667.1:g.112043015C>G	GRCh37
NC_000005.8:g.112070914C>G	NCBI36
NG_008481.4:g.19798C>G , LRG_130:g.19798C>G