Canonical Allele Identifier: CA100366657

Gene: LINC01094

Linked Data

• dbSNP Id: rs949963228
• MyVariant Identifiers: chr4:g.79589127A>G (hg19) ; chr4:g.78667973A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78667973A>G , CM000666.2:g.78667973A>G	GRCh38
NC_000004.11:g.79589127A>G , CM000666.1:g.79589127A>G	GRCh37
NC_000004.10:g.79808151A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038303.1:n.473+4962A>G
NR_038304.1:n.473+4962A>G
NR_038305.1:n.380-5370A>G
NR_038306.1:n.380-12788A>G
NR_038307.1:n.364+4962A>G
NR_038308.1:n.325+5001A>G