Canonical Allele Identifier: CA2140112667
Gene: LINC01500 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.58899597G>C , CM000676.2:g.58899597G>C GRCh38
NC_000014.8:g.59366315G>C , CM000676.1:g.59366315G>C GRCh37
NC_000014.7:g.58436068G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110547.1:n.457+5266G>C