Canonical Allele Identifier: CA2709892790
Gene: LINC02208 HGNC NCBI

Linked Data

dbSNP Id: rs2112771372
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.118365687T>A , CM000667.2:g.118365687T>A GRCh38
NC_000005.9:g.117701382T>A , CM000667.1:g.117701382T>A GRCh37
NC_000005.8:g.117729281T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104610.1:n.2658-14180A>T
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Search 100 bp 3'