Canonical Allele Identifier: CA2573138730

Gene:

Linked Data

• ClinVar Variation Id: 1410279
• ClinVar RCV Id: RCV002557634
• dbSNP Id: rs2149627907

Genomic Alleles

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