Canonical Allele Identifier: CA2605608517
Gene: LINC02006 HGNC NCBI

Linked Data

dbSNP Id: rs2108030221

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.153632253del , CM000665.2:g.153632253del GRCh38
NC_000003.11:g.153350042del , CM000665.1:g.153350042del GRCh37
NC_000003.10:g.154832732del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924593.1:n.363-27507del
XR_924594.1:n.60+25818del
NR_146713.1:n.161-27507del