Canonical Allele Identifier: CA13360032
Gene: LINC02664 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.31223169T>C , CM000672.2:g.31223169T>C GRCh38
NC_000010.10:g.31512098T>C , CM000672.1:g.31512098T>C GRCh37
NC_000010.9:g.31552104T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_242751.2:n.490+34970T>C
NR_134478.1:n.317+34970T>C
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