Canonical Allele Identifier: CA552690291

Gene: LINC01094

Linked Data

• dbSNP Id: rs1427598027
• gnomAD v2: 4-79588930-CT-C
• gnomAD v3: 4-78667776-CT-C
• gnomAD v4: 4-78667776-CT-C
• MyVariant Identifiers: chr4:g.79588931del (hg19) ; chr4:g.78667777del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78667783del , CM000666.2:g.78667783del	GRCh38
NC_000004.11:g.79588937del , CM000666.1:g.79588937del	GRCh37
NC_000004.10:g.79807961del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038303.1:n.473+4772del
NR_038304.1:n.473+4772del
NR_038305.1:n.380-5560del
NR_038306.1:n.380-12978del
NR_038307.1:n.364+4772del
NR_038308.1:n.325+4811del