Canonical Allele Identifier: CA774554972

Gene: LINC01483

Linked Data

• dbSNP Id: rs1394240507
• gnomAD v3: 17-69854569-AG-A
• gnomAD v4: 17-69854569-AG-A
• MyVariant Identifiers: chr17:g.67850711del (hg19) ; chr17:g.69854570del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.69854570del , CM000679.2:g.69854570del	GRCh38
NC_000017.10:g.67850711del , CM000679.1:g.67850711del	GRCh37
NC_000017.9:g.65362306del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_109971.1:n.363+9084del
NR_109972.1:n.363+9084del