Canonical Allele Identifier: CA2140086947
Gene: LINC01500 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.58867472G= , CM000676.2:g.58867472G= GRCh38
NC_000014.8:g.59334190G= , CM000676.1:g.59334190G= GRCh37
NC_000014.7:g.58403943G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110547.1:n.269-26671G=