Canonical Allele Identifier: CA584791096

Gene:

Linked Data

• dbSNP Id: rs1382389837
• gnomAD v2: 8-123408501-AG-A
• gnomAD v3: 8-122396262-AG-A
• gnomAD v4: 8-122396262-AG-A
• MyVariant Identifiers: chr8:g.123408502del (hg19) ; chr8:g.122396263del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.122396266del , CM000670.2:g.122396266del	GRCh38
NC_000008.10:g.123408505del , CM000670.1:g.123408505del	GRCh37
NC_000008.9:g.123477686del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_928599.1:n.152+2909del
XR_928599.3:n.152+2909del