Canonical Allele Identifier: CA11251900
Gene: LINC01890 HGNC NCBI
LINC01888 HGNC NCBI

Linked Data

dbSNP Id: rs10496166
gnomAD v2: 2-69063909-G-A
gnomAD v3: 2-68836777-G-A
gnomAD v4: 2-68836777-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.68836777G>A , CM000664.2:g.68836777G>A GRCh38
NC_000002.11:g.69063909G>A , CM000664.1:g.69063909G>A GRCh37
NC_000002.10:g.68917413G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940226.1:n.431C>T (LINC01890)
XR_001739529.2:n.612C>T (LINC01890)
XR_001739530.1:n.862-605G>A (LINC01888)
XR_940226.3:n.612C>T (LINC01890)