Canonical Allele Identifier: CA15284031
Gene: LINC02006 HGNC NCBI

Linked Data

dbSNP Id: rs7623788

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.153632327A>G , CM000665.2:g.153632327A>G GRCh38
NC_000003.11:g.153350116A>G , CM000665.1:g.153350116A>G GRCh37
NC_000003.10:g.154832806A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_924593.1:n.363-27582T>C
XR_924594.1:n.60+25743T>C
NR_146713.1:n.161-27582T>C