Canonical Allele Identifier: CA2140086923
Gene: LINC01500 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.58867453C= , CM000676.2:g.58867453C= GRCh38
NC_000014.8:g.59334171C= , CM000676.1:g.59334171C= GRCh37
NC_000014.7:g.58403924C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110547.1:n.269-26690C=