Canonical Allele Identifier: CA1300329686
Gene: LINC01876 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156031988C= , CM000664.2:g.156031988C= GRCh38
NC_000002.11:g.156888500C= , CM000664.1:g.156888500C= GRCh37
NC_000002.10:g.156596746C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110249.2:n.155-7412G=
NR_110250.2:n.155-7381G=