Canonical Allele Identifier: CA1573442156

Gene:

Linked Data

• ClinVar Variation Id: 1047277
• ClinVar RCV Id: RCV002242433
• dbSNP Id: rs1750548351

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707325C>G , CM000667.2:g.112707325C>G	GRCh38
NC_000005.9:g.112043022C>G , CM000667.1:g.112043022C>G	GRCh37
NC_000005.8:g.112070921C>G	NCBI36
NG_008481.4:g.19805C>G , LRG_130:g.19805C>G