Canonical Allele Identifier: CA1470816780
Gene: LINC01088 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.79043433A= , CM000666.2:g.79043433A= GRCh38
NC_000004.11:g.79964587A= , CM000666.1:g.79964587A= GRCh37
NC_000004.10:g.80183611A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038342.1:n.183-42663A=