Canonical Allele Identifier: CA1412084108
Gene: LINC02006 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.153632390C= , CM000665.2:g.153632390C= GRCh38
NC_000003.11:g.153350179C= , CM000665.1:g.153350179C= GRCh37
NC_000003.10:g.154832869C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_924593.1:n.363-27645G=
XR_924594.1:n.60+25680G=
NR_146713.1:n.161-27645G=
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