Canonical Allele Identifier: CA2580072222

Gene:

Linked Data

• ClinVar Variation Id: 2146342
• ClinVar RCV Id: RCV003074512

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707347C>A , CM000667.2:g.112707347C>A	GRCh38
NC_000005.9:g.112043044C>A , CM000667.1:g.112043044C>A	GRCh37
NC_000005.8:g.112070943C>A	NCBI36
NG_008481.4:g.19827C>A , LRG_130:g.19827C>A