Canonical Allele Identifier: CA2758963298
Gene: LINC02006 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.153632228A>C , CM000665.2:g.153632228A>C GRCh38
NC_000003.11:g.153350017A>C , CM000665.1:g.153350017A>C GRCh37
NC_000003.10:g.154832707A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924593.1:n.363-27483T>G
XR_924594.1:n.60+25842T>G
NR_146713.1:n.161-27483T>G