Canonical Allele Identifier: CA1333499350
Gene: LINC01807 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.228646150A= , CM000664.2:g.228646150A= GRCh38
NC_000002.11:g.229510866A= , CM000664.1:g.229510866A= GRCh37
NC_000002.10:g.229219110A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923977.1:n.39+98493T=