Canonical Allele Identifier: CA1451697729
Gene: LINC01258 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.38490214C= , CM000666.2:g.38490214C= GRCh38
NC_000004.11:g.38491835C= , CM000666.1:g.38491835C= GRCh37
NC_000004.10:g.38168230C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110951.1:n.184+3779G=