Canonical Allele Identifier: CA1573442279

Gene:

Linked Data

• ClinVar Variation Id: 1002324
• ClinVar RCV Id: RCV003538645
• dbSNP Id: rs1427438975
• gnomAD v4: 5-112707420-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707420C>A , CM000667.2:g.112707420C>A	GRCh38
NC_000005.9:g.112043117C>A , CM000667.1:g.112043117C>A	GRCh37
NC_000005.8:g.112071016C>A	NCBI36
NG_008481.4:g.19900C>A , LRG_130:g.19900C>A