Canonical Allele Identifier: CA576417280

Gene:

Linked Data

• dbSNP Id: rs66714162
• gnomAD v2: 7-99593021-CTT-C
• gnomAD v3: 7-99995398-CTT-C
• gnomAD v4: 7-99995398-CTT-C
• MyVariant Identifiers: chr7:g.99593025_99593026del (hg19) ; chr7:g.99593022_99593023del (hg19) ; chr7:g.99995402_99995403del (hg38) ; chr7:g.99995399_99995400del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99995424_99995425del , CM000669.2:g.99995424_99995425del	GRCh38
NC_000007.13:g.99593047_99593048del , CM000669.1:g.99593047_99593048del	GRCh37
NC_000007.12:g.99430983_99430984del	NCBI36