Canonical Allele Identifier: CA2086427257
Gene: LINC00598 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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