Canonical Allele Identifier: CA1300348905
Gene: LINC01876 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156077041A= , CM000664.2:g.156077041A= GRCh38
NC_000002.11:g.156933553A= , CM000664.1:g.156933553A= GRCh37
NC_000002.10:g.156641799A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110249.2:n.155-52465T=
NR_110250.2:n.155-52434T=