Canonical Allele Identifier: CA802056892

Gene:

Linked Data

• ClinVar Variation Id: 665946
• ClinVar RCV Id: RCV003768544
• dbSNP Id: rs1345543059
• gnomAD v3: 5-112707413-A-G
• gnomAD v4: 5-112707413-A-G
• MyVariant Identifiers: chr5:g.112043110A>G (hg19) ; chr5:g.112707413A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707413A>G , CM000667.2:g.112707413A>G	GRCh38
NC_000005.9:g.112043110A>G , CM000667.1:g.112043110A>G	GRCh37
NC_000005.8:g.112071009A>G	NCBI36
NG_008481.4:g.19893A>G , LRG_130:g.19893A>G