Canonical Allele Identifier: CA2499217373

Gene:

Linked Data

• ClinVar Variation Id: 1052172
• ClinVar RCV Id: RCV002242529
• dbSNP Id: rs960491839

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707407C>A , CM000667.2:g.112707407C>A	GRCh38
NC_000005.9:g.112043104C>A , CM000667.1:g.112043104C>A	GRCh37
NC_000005.8:g.112071003C>A	NCBI36
NG_008481.4:g.19887C>A , LRG_130:g.19887C>A