Canonical Allele Identifier: CA1412084107
Gene: LINC02006 HGNC NCBI

Linked Data

dbSNP Id: rs1713916279

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.153632389_153632390del , CM000665.2:g.153632389_153632390del GRCh38
NC_000003.11:g.153350178_153350179del , CM000665.1:g.153350178_153350179del GRCh37
NC_000003.10:g.154832868_154832869del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924593.1:n.363-27644_363-27643del
XR_924594.1:n.60+25681_60+25682del
NR_146713.1:n.161-27644_161-27643del