Canonical Allele Identifier: CA802056844

Gene:

Linked Data

• ClinVar Variation Id: 1003986
• ClinVar RCV Id: RCV003538648
• dbSNP Id: rs1316145446
• gnomAD v3: 5-112707388-CAG-C
• gnomAD v4: 5-112707388-CAG-C
• MyVariant Identifiers: chr5:g.112043086_112043087del (hg19) ; chr5:g.112707389_112707390del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707390_112707391del , CM000667.2:g.112707390_112707391del	GRCh38
NC_000005.9:g.112043087_112043088del , CM000667.1:g.112043087_112043088del	GRCh37
NC_000005.8:g.112070986_112070987del	NCBI36
NG_008481.4:g.19870_19871del , LRG_130:g.19870_19871del