Canonical Allele Identifier: CA1064495928

Gene: LINC01094

Linked Data

• dbSNP Id: rs1724943813
• gnomAD v3: 4-78667726-G-T
• gnomAD v4: 4-78667726-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78667726G>T , CM000666.2:g.78667726G>T	GRCh38
NC_000004.11:g.79588880G>T , CM000666.1:g.79588880G>T	GRCh37
NC_000004.10:g.79807904G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_038303.1:n.473+4715G>T
NR_038304.1:n.473+4715G>T
NR_038305.1:n.380-5617G>T
NR_038306.1:n.380-13035G>T
NR_038307.1:n.364+4715G>T
NR_038308.1:n.325+4754G>T