Canonical Allele Identifier: CA15286054
Gene: LINC02006 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.153754374T>G , CM000665.2:g.153754374T>G GRCh38
NC_000003.11:g.153472163T>G , CM000665.1:g.153472163T>G GRCh37
NC_000003.10:g.154954853T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924593.1:n.310-23567A>C
NR_146713.1:n.24+8129A>C
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