Canonical Allele Identifier: CA59124324
Gene: LINC01876 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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