Canonical Allele Identifier: CA2758963299
Gene: LINC02006 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.153632238T>G , CM000665.2:g.153632238T>G GRCh38
NC_000003.11:g.153350027T>G , CM000665.1:g.153350027T>G GRCh37
NC_000003.10:g.154832717T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924593.1:n.363-27493A>C
XR_924594.1:n.60+25832A>C
NR_146713.1:n.161-27493A>C