Canonical Allele Identifier: CA561890095

Gene:

Linked Data

• ClinVar Variation Id: 469874
• ClinVar RCV Id: RCV003742660
• dbSNP Id: rs1313658633
• gnomAD v2: 5-112043139-C-A
• gnomAD v3: 5-112707442-C-A
• gnomAD v4: 5-112707442-C-A
• MyVariant Identifiers: chr5:g.112043139C>A (hg19) ; chr5:g.112707442C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707442C>A , CM000667.2:g.112707442C>A	GRCh38
NC_000005.9:g.112043139C>A , CM000667.1:g.112043139C>A	GRCh37
NC_000005.8:g.112071038C>A	NCBI36
NG_008481.4:g.19922C>A , LRG_130:g.19922C>A