Canonical Allele Identifier: CA1314064486
Gene: LINC01473 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.186079957A= , CM000664.2:g.186079957A= GRCh38
NC_000002.11:g.186944684A= , CM000664.1:g.186944684A= GRCh37
NC_000002.10:g.186652929A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110218.1:n.172+1373T=