Canonical Allele Identifier: CA1573442153

Gene:

Linked Data

• ClinVar Variation Id: 1001434
• ClinVar RCV Id: RCV002541844
• dbSNP Id: rs1750548089

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707315C>T , CM000667.2:g.112707315C>T	GRCh38
NC_000005.9:g.112043012C>T , CM000667.1:g.112043012C>T	GRCh37
NC_000005.8:g.112070911C>T	NCBI36
NG_008481.4:g.19795C>T , LRG_130:g.19795C>T