Canonical Allele Identifier: CA802056793

Gene:

Linked Data

• ClinVar Variation Id: 639350
• ClinVar RCV Id: RCV003535852
• dbSNP Id: rs1232455560
• gnomAD v3: 5-112707346-G-A
• gnomAD v4: 5-112707346-G-A
• MyVariant Identifiers: chr5:g.112043043G>A (hg19) ; chr5:g.112707346G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707346G>A , CM000667.2:g.112707346G>A	GRCh38
NC_000005.9:g.112043043G>A , CM000667.1:g.112043043G>A	GRCh37
NC_000005.8:g.112070942G>A	NCBI36
NG_008481.4:g.19826G>A , LRG_130:g.19826G>A