Canonical Allele Identifier: CA2086427256
Community Standard Title: NC_000013.11:g.40439840T=
Gene: LINC00598 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40439840T= , CM000675.2:g.40439840T= GRCh38
NC_000013.10:g.41013977T= , CM000675.1:g.41013977T= GRCh37
NC_000013.9:g.39911977T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024506.1:n.663+20442A=
NR_024507.2:n.803+11224A=