Canonical Allele Identifier: CA576771101

Gene:

Linked Data

• dbSNP Id: rs58630561
• gnomAD v2: 7-109152498-CTTT-C
• gnomAD v3: 7-109512441-CTTT-C
• gnomAD v4: 7-109512441-CTTT-C
• MyVariant Identifiers: chr7:g.109152501_109152503del (hg19) ; chr7:g.109152499_109152501del (hg19) ; chr7:g.109512444_109512446del (hg38) ; chr7:g.109512442_109512444del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.109512456_109512458del , CM000669.2:g.109512456_109512458del	GRCh38
NC_000007.13:g.109152513_109152515del , CM000669.1:g.109152513_109152515del	GRCh37
NC_000007.12:g.108939749_108939751del	NCBI36