Canonical Allele Identifier: CA658655869

Gene:

Linked Data

• ClinVar Variation Id: 469891
• ClinVar RCV Id: RCV003742663
• dbSNP Id: rs1554060123
• gnomAD v4: 5-112707371-A-G
• MyVariant Identifiers: chr5:g.112043068A>G (hg19) ; chr5:g.112707371A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707371A>G , CM000667.2:g.112707371A>G	GRCh38
NC_000005.9:g.112043068A>G , CM000667.1:g.112043068A>G	GRCh37
NC_000005.8:g.112070967A>G	NCBI36
NG_008481.4:g.19851A>G , LRG_130:g.19851A>G