Canonical Allele Identifier: CA124924645

Gene:

Linked Data

• ClinVar Variation Id: 469878
• ClinVar RCV Id: RCV003537058
• dbSNP Id: rs372923973
• gnomAD v2: 5-112043115-A-G
• gnomAD v3: 5-112707418-A-G
• gnomAD v4: 5-112707418-A-G
• MyVariant Identifiers: chr5:g.112043115A>G (hg19) ; chr5:g.112707418A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707418A>G , CM000667.2:g.112707418A>G	GRCh38
NC_000005.9:g.112043115A>G , CM000667.1:g.112043115A>G	GRCh37
NC_000005.8:g.112071014A>G	NCBI36
NG_008481.4:g.19898A>G , LRG_130:g.19898A>G