Canonical Allele Identifier: CA647951238
Gene: LINC02006 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.153632239C>A , CM000665.2:g.153632239C>A GRCh38
NC_000003.11:g.153350028C>A , CM000665.1:g.153350028C>A GRCh37
NC_000003.10:g.154832718C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924593.1:n.363-27494G>T
XR_924594.1:n.60+25831G>T
NR_146713.1:n.161-27494G>T