Canonical Allele Identifier: CA100366652

Gene: LINC01094

Linked Data

• dbSNP Id: rs533552563
• gnomAD v2: 4-79589103-G-A
• gnomAD v3: 4-78667949-G-A
• gnomAD v4: 4-78667949-G-A
• MyVariant Identifiers: chr4:g.79589103G>A (hg19) ; chr4:g.78667949G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78667949G>A , CM000666.2:g.78667949G>A	GRCh38
NC_000004.11:g.79589103G>A , CM000666.1:g.79589103G>A	GRCh37
NC_000004.10:g.79808127G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038303.1:n.473+4938G>A
NR_038304.1:n.473+4938G>A
NR_038305.1:n.380-5394G>A
NR_038306.1:n.380-12812G>A
NR_038307.1:n.364+4938G>A
NR_038308.1:n.325+4977G>A