Canonical Allele Identifier: CA1791698879
Gene: LINC01592 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.69080145G= , CM000670.2:g.69080145G= GRCh38
NC_000008.10:g.69992380G= , CM000670.1:g.69992380G= GRCh37
NC_000008.9:g.70154934G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_039986.1:n.194-11596C=