Canonical Allele Identifier: CA1055103766
Gene: LINC02006 HGNC NCBI

Linked Data

dbSNP Id: rs957223133

Genomic Alleles

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

Transcript Alleles

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