Canonical Allele Identifier: CA11978063

Gene:

Linked Data

• ClinVar Variation Id: 506394
• ClinVar RCV Id: RCV000607512
• dbSNP Id: rs116505416
• gnomAD v2: 5-112042999-A-G
• gnomAD v3: 5-112707302-A-G
• gnomAD v4: 5-112707302-A-G
• MyVariant Identifiers: chr5:g.112042999A>G (hg19) ; chr5:g.112707302A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707302A>G , CM000667.2:g.112707302A>G	GRCh38
NC_000005.9:g.112042999A>G , CM000667.1:g.112042999A>G	GRCh37
NC_000005.8:g.112070898A>G	NCBI36
NG_008481.4:g.19782A>G , LRG_130:g.19782A>G