Canonical Allele Identifier: CA1412084049
Gene: LINC02006 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.153632250C= , CM000665.2:g.153632250C= GRCh38
NC_000003.11:g.153350039C= , CM000665.1:g.153350039C= GRCh37
NC_000003.10:g.154832729C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924593.1:n.363-27505G=
XR_924594.1:n.60+25820G=
NR_146713.1:n.161-27505G=