Canonical Allele Identifier: CA1297593733
Community Standard Title: NC_000002.12:g.150269889G=
Gene: LINC01818 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.150269889G= , CM000664.2:g.150269889G= GRCh38
NC_000002.11:g.151126403G= , CM000664.1:g.151126403G= GRCh37
NC_000002.10:g.150834649G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923469.1:n.228+55477G=
XR_923469.2:n.249+55477G=