Canonical Allele Identifier: CA2150809734
Gene: LINC02301 HGNC NCBI

Linked Data

dbSNP Id: rs1893905286
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.82739721A>G , CM000676.2:g.82739721A>G GRCh38
NC_000014.8:g.83206065A>G , CM000676.1:g.83206065A>G GRCh37
NC_000014.7:g.82275818A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944088.1:n.362-978A>G
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