Canonical Allele Identifier: CA124924417

Gene:

Linked Data

• ClinVar Variation Id: 1195720
• ClinVar RCV Id: RCV001558910
• dbSNP Id: rs115535112
• gnomAD v2: 5-112042873-C-T
• gnomAD v3: 5-112707176-C-T
• gnomAD v4: 5-112707176-C-T
• MyVariant Identifiers: chr5:g.112042873C>T (hg19) ; chr5:g.112707176C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707176C>T , CM000667.2:g.112707176C>T	GRCh38
NC_000005.9:g.112042873C>T , CM000667.1:g.112042873C>T	GRCh37
NC_000005.8:g.112070772C>T	NCBI36
NG_008481.4:g.19656C>T , LRG_130:g.19656C>T