Canonical Allele Identifier: CA1514142876
Gene: LINC02268 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.174106410T= , CM000666.2:g.174106410T= GRCh38
NC_000004.11:g.175027561T= , CM000666.1:g.175027561T= GRCh37
NC_000004.10:g.175264136T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125896.1:n.276-8581A=
XR_939484.1:n.877+18771T=
XR_939485.1:n.877+18771T=
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