Canonical Allele Identifier: CA658655870

Gene:

Linked Data

• ClinVar Variation Id: 469888
• ClinVar RCV Id: RCV002231946
• dbSNP Id: rs1554060128
• gnomAD v4: 5-112707384-G-A
• MyVariant Identifiers: chr5:g.112043081G>A (hg19) ; chr5:g.112707384G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707384G>A , CM000667.2:g.112707384G>A	GRCh38
NC_000005.9:g.112043081G>A , CM000667.1:g.112043081G>A	GRCh37
NC_000005.8:g.112070980G>A	NCBI36
NG_008481.4:g.19864G>A , LRG_130:g.19864G>A