Canonical Allele Identifier: CA561890079

Gene:

Linked Data

• ClinVar Variation Id: 469890
• ClinVar RCV Id: RCV003537059
• dbSNP Id: rs1218378018
• gnomAD v2: 5-112043073-T-C
• gnomAD v3: 5-112707376-T-C
• gnomAD v4: 5-112707376-T-C
• MyVariant Identifiers: chr5:g.112043073T>C (hg19) ; chr5:g.112707376T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707376T>C , CM000667.2:g.112707376T>C	GRCh38
NC_000005.9:g.112043073T>C , CM000667.1:g.112043073T>C	GRCh37
NC_000005.8:g.112070972T>C	NCBI36
NG_008481.4:g.19856T>C , LRG_130:g.19856T>C