Canonical Allele Identifier: CA15702840
Gene: LINC02699 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.25766084T>C , CM000673.2:g.25766084T>C GRCh38
NC_000011.9:g.25787631T>C , CM000673.1:g.25787631T>C GRCh37
NC_000011.8:g.25744207T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_931132.1:n.77-4387T>C
XR_931134.1:n.170-11610T>C
XR_931135.1:n.77-11610T>C
XR_931136.1:n.77-4387T>C
XR_931132.3:n.75-4387T>C
XR_931135.2:n.81-11610T>C
XR_931136.3:n.75-4387T>C
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