Canonical Allele Identifier: CA1573442208

Gene:

Linked Data

• ClinVar Variation Id: 1495121
• ClinVar RCV Id: RCV003773274
• dbSNP Id: rs929883108

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707366T>G , CM000667.2:g.112707366T>G	GRCh38
NC_000005.9:g.112043063T>G , CM000667.1:g.112043063T>G	GRCh37
NC_000005.8:g.112070962T>G	NCBI36
NG_008481.4:g.19846T>G , LRG_130:g.19846T>G