Canonical Allele Identifier: CA2054860055
Community Standard Title: NC_000012.12:g.92311428A=
Gene: LINC02391 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.92311428A= , CM000674.2:g.92311428A= GRCh38
NC_000012.11:g.92705204A= , CM000674.1:g.92705204A= GRCh37
NC_000012.10:g.91229335A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011539067.1:c.47-16926T= XP_011537369.1:n.47-16926T=
XR_001749257.2:n.414-38812T=
XR_001749258.2:n.414-42449T=
XR_001749259.2:n.414-22821T=
XR_945204.1:n.413-42449T=