Canonical Allele Identifier: CA1140067335
Gene: LINC02801 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.87239348A= , CM000663.2:g.87239348A= GRCh38
NC_000001.10:g.87705031A= , CM000663.1:g.87705031A= GRCh37
NC_000001.9:g.87477619A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001290053.1:c.1-4267A= NP_001276982.1:n.1-4267A=
XM_011542525.1:c.403+12202A= XP_011540827.1:n.403+12202A=
XM_016999997.1:c.1-4267A= XP_016855486.1:n.1-4267A=
NR_167752.1:n.299-4267A=