Canonical Allele Identifier: CA2709892811
Gene: LINC02208 HGNC NCBI

Linked Data

dbSNP Id: rs2112771477
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.118365850T>G , CM000667.2:g.118365850T>G GRCh38
NC_000005.9:g.117701545T>G , CM000667.1:g.117701545T>G GRCh37
NC_000005.8:g.117729444T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104610.1:n.2658-14343A>C
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Search 100 bp 3'