Canonical Allele Identifier: CA2573138729

Gene:

Linked Data

• ClinVar Variation Id: 1491765
• ClinVar RCV Id: RCV003773243
• dbSNP Id: rs2149627907

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707316A>G , CM000667.2:g.112707316A>G	GRCh38
NC_000005.9:g.112043013A>G , CM000667.1:g.112043013A>G	GRCh37
NC_000005.8:g.112070912A>G	NCBI36
NG_008481.4:g.19796A>G , LRG_130:g.19796A>G