Canonical Allele Identifier: CA2709892809
Gene: LINC02208 HGNC NCBI

Linked Data

dbSNP Id: rs2112771460
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.118365828A>G , CM000667.2:g.118365828A>G GRCh38
NC_000005.9:g.117701523A>G , CM000667.1:g.117701523A>G GRCh37
NC_000005.8:g.117729422A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104610.1:n.2658-14321T>C
Search 100 bp 5'
Search 100 bp 3'