Canonical Allele Identifier: CA561890082

Gene:

Linked Data

• ClinVar Variation Id: 1004961
• ClinVar RCV Id: RCV003652135
• dbSNP Id: rs1243549213
• gnomAD v2: 5-112043075-G-A
• gnomAD v3: 5-112707378-G-A
• gnomAD v4: 5-112707378-G-A
• MyVariant Identifiers: chr5:g.112043075G>A (hg19) ; chr5:g.112707378G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707378G>A , CM000667.2:g.112707378G>A	GRCh38
NC_000005.9:g.112043075G>A , CM000667.1:g.112043075G>A	GRCh37
NC_000005.8:g.112070974G>A	NCBI36
NG_008481.4:g.19858G>A , LRG_130:g.19858G>A