Canonical Allele Identifier: CA802056903

Gene:

Linked Data

• ClinVar Variation Id: 639419
• ClinVar RCV Id: RCV002535866
• dbSNP Id: rs1427438975
• gnomAD v3: 5-112707420-C-G
• gnomAD v4: 5-112707420-C-G
• MyVariant Identifiers: chr5:g.112043117C>G (hg19) ; chr5:g.112707420C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707420C>G , CM000667.2:g.112707420C>G	GRCh38
NC_000005.9:g.112043117C>G , CM000667.1:g.112043117C>G	GRCh37
NC_000005.8:g.112071016C>G	NCBI36
NG_008481.4:g.19900C>G , LRG_130:g.19900C>G