Canonical Allele Identifier: CA100366636

Gene: LINC01094

Linked Data

• dbSNP Id: rs905499493
• MyVariant Identifiers: chr4:g.79588942C>T (hg19) ; chr4:g.78667788C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78667788C>T , CM000666.2:g.78667788C>T	GRCh38
NC_000004.11:g.79588942C>T , CM000666.1:g.79588942C>T	GRCh37
NC_000004.10:g.79807966C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038303.1:n.473+4777C>T
NR_038304.1:n.473+4777C>T
NR_038305.1:n.380-5555C>T
NR_038306.1:n.380-12973C>T
NR_038307.1:n.364+4777C>T
NR_038308.1:n.325+4816C>T