Canonical Allele Identifier: CA2042320737
Community Standard Title: NC_000012.12:g.64897514G=
Gene: LINC02389 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.64897514G= , CM000674.2:g.64897514G= GRCh38
NC_000012.11:g.65291294G= , CM000674.1:g.65291294G= GRCh37
NC_000012.10:g.63577561G= NCBI36
NG_027727.1:g.18741G=

Transcript Alleles

HGVS Amino-acid Change
NR_033988.1:n.93-3063G=
ENST00000674281.1:c.*1471+12214G= ENSP00000501395.1:n.*1471+12214G=