Canonical Allele Identifier: CA2731546193
Gene: LINC02883 HGNC NCBI

Linked Data

dbSNP Id: rs2151802221
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.85756948T>A , CM000677.2:g.85756948T>A GRCh38
NC_000015.9:g.86300179T>A , CM000677.1:g.86300179T>A GRCh37
NC_000015.8:g.84101183T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_120366.1:n.419+936A>T
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