Canonical Allele Identifier: CA2499217366

Gene:

Linked Data

• ClinVar Variation Id: 1062895
• ClinVar RCV Id: RCV003538762
• dbSNP Id: rs2149628038

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707344C>G , CM000667.2:g.112707344C>G	GRCh38
NC_000005.9:g.112043041C>G , CM000667.1:g.112043041C>G	GRCh37
NC_000005.8:g.112070940C>G	NCBI36
NG_008481.4:g.19824C>G , LRG_130:g.19824C>G