Canonical Allele Identifier: CA798766784

Gene: LINC01094

Linked Data

• dbSNP Id: rs1221999709
• gnomAD v3: 4-78667811-T-A
• gnomAD v4: 4-78667811-T-A
• MyVariant Identifiers: chr4:g.79588965T>A (hg19) ; chr4:g.78667811T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78667811T>A , CM000666.2:g.78667811T>A	GRCh38
NC_000004.11:g.79588965T>A , CM000666.1:g.79588965T>A	GRCh37
NC_000004.10:g.79807989T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038303.1:n.473+4800T>A
NR_038304.1:n.473+4800T>A
NR_038305.1:n.380-5532T>A
NR_038306.1:n.380-12950T>A
NR_038307.1:n.364+4800T>A
NR_038308.1:n.325+4839T>A