Canonical Allele Identifier: CA124924532

Gene:

Linked Data

• ClinVar Variation Id: 469903
• ClinVar RCV Id: RCV003537064
• dbSNP Id: rs185951958
• gnomAD v2: 5-112043009-C-T
• gnomAD v3: 5-112707312-C-T
• gnomAD v4: 5-112707312-C-T
• MyVariant Identifiers: chr5:g.112043009C>T (hg19) ; chr5:g.112707312C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707312C>T , CM000667.2:g.112707312C>T	GRCh38
NC_000005.9:g.112043009C>T , CM000667.1:g.112043009C>T	GRCh37
NC_000005.8:g.112070908C>T	NCBI36
NG_008481.4:g.19792C>T , LRG_130:g.19792C>T