Canonical Allele Identifier: CA1300345327
Gene: LINC01876 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156068774A>G , CM000664.2:g.156068774A>G GRCh38
NC_000002.11:g.156925286A>G , CM000664.1:g.156925286A>G GRCh37
NC_000002.10:g.156633532A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110249.2:n.155-44198T>C
NR_110250.2:n.155-44167T>C