Canonical Allele Identifier: CA1300329687
Gene: LINC01876 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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