Canonical Allele Identifier: CA1412084058
Gene: LINC02006 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.153632270G= , CM000665.2:g.153632270G= GRCh38
NC_000003.11:g.153350059G= , CM000665.1:g.153350059G= GRCh37
NC_000003.10:g.154832749G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924593.1:n.363-27525C=
XR_924594.1:n.60+25800C=
NR_146713.1:n.161-27525C=