Canonical Allele Identifier: CA1514142863
Gene: LINC02268 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.174106388C= , CM000666.2:g.174106388C= GRCh38
NC_000004.11:g.175027539C= , CM000666.1:g.175027539C= GRCh37
NC_000004.10:g.175264114C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125896.1:n.276-8559G=
XR_939484.1:n.877+18749C=
XR_939485.1:n.877+18749C=
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