Canonical Allele Identifier: CA2581831487
Gene: LINC01173 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.234706553A>T , CM000664.2:g.234706553A>T GRCh38
NC_000002.11:g.235615197A>T , CM000664.1:g.235615197A>T GRCh37
NC_000002.10:g.235279936A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_132376.1:n.201+10805A>T