Canonical Allele Identifier: CA1573442357

Gene:

Linked Data

• ClinVar Variation Id: 1041055
• ClinVar RCV Id: RCV003770952
• dbSNP Id: rs1750567665

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707487C>G , CM000667.2:g.112707487C>G	GRCh38
NC_000005.9:g.112043184C>G , CM000667.1:g.112043184C>G	GRCh37
NC_000005.8:g.112071083C>G	NCBI36
NG_008481.4:g.19967C>G , LRG_130:g.19967C>G