Canonical Allele Identifier: CA1336338533
Gene: LINC01173 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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