Canonical Allele Identifier: CA426450454
Gene: LINC01890 HGNC NCBI
LINC01888 HGNC NCBI

Linked Data

dbSNP Id: rs10496166
MyVariant Identifiers: chr2:g.69063909G>C (hg19)

Genomic Alleles

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

Transcript Alleles

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