Canonical Allele Identifier: CA1573442201

Gene:

Linked Data

• ClinVar Variation Id: 1036580
• ClinVar RCV Id: RCV003154002
• dbSNP Id: rs1750551783

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707361C>G , CM000667.2:g.112707361C>G	GRCh38
NC_000005.9:g.112043058C>G , CM000667.1:g.112043058C>G	GRCh37
NC_000005.8:g.112070957C>G	NCBI36
NG_008481.4:g.19841C>G , LRG_130:g.19841C>G