Canonical Allele Identifier: CA100366626

Gene: LINC01094

Linked Data

• dbSNP Id: rs574602461
• gnomAD v3: 4-78667702-G-C
• gnomAD v4: 4-78667702-G-C
• MyVariant Identifiers: chr4:g.79588856G>C (hg19) ; chr4:g.78667702G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78667702G>C , CM000666.2:g.78667702G>C	GRCh38
NC_000004.11:g.79588856G>C , CM000666.1:g.79588856G>C	GRCh37
NC_000004.10:g.79807880G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038303.1:n.473+4691G>C
NR_038304.1:n.473+4691G>C
NR_038305.1:n.380-5641G>C
NR_038306.1:n.380-13059G>C
NR_038307.1:n.364+4691G>C
NR_038308.1:n.325+4730G>C