Canonical Allele Identifier: CA1412084086
Gene: LINC02006 HGNC NCBI

Linked Data

dbSNP Id: rs1713914713

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.153632330G>A , CM000665.2:g.153632330G>A GRCh38
NC_000003.11:g.153350119G>A , CM000665.1:g.153350119G>A GRCh37
NC_000003.10:g.154832809G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924593.1:n.363-27585C>T
XR_924594.1:n.60+25740C>T
NR_146713.1:n.161-27585C>T