Canonical Allele Identifier: CA2573138756

Gene:

Linked Data

• ClinVar Variation Id: 1372761
• ClinVar RCV Id: RCV003745364
• dbSNP Id: rs2149628636

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707423A>C , CM000667.2:g.112707423A>C	GRCh38
NC_000005.9:g.112043120A>C , CM000667.1:g.112043120A>C	GRCh37
NC_000005.8:g.112071019A>C	NCBI36
NG_008481.4:g.19903A>C , LRG_130:g.19903A>C