Canonical Allele Identifier: CA798766943

Gene: LINC01094

Linked Data

• dbSNP Id: rs1213127768
• MyVariant Identifiers: chr4:g.79589158T>G (hg19) ; chr4:g.78668004T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78668004T>G , CM000666.2:g.78668004T>G	GRCh38
NC_000004.11:g.79589158T>G , CM000666.1:g.79589158T>G	GRCh37
NC_000004.10:g.79808182T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038303.1:n.473+4993T>G
NR_038304.1:n.473+4993T>G
NR_038305.1:n.380-5339T>G
NR_038306.1:n.380-12757T>G
NR_038307.1:n.364+4993T>G
NR_038308.1:n.325+5032T>G