Canonical Allele Identifier: CA1576425899
Gene: LINC02208 HGNC NCBI

Linked Data

dbSNP Id: rs1753182103
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.118365860T>C , CM000667.2:g.118365860T>C GRCh38
NC_000005.9:g.117701555T>C , CM000667.1:g.117701555T>C GRCh37
NC_000005.8:g.117729454T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104610.1:n.2658-14353A>G
Search 100 bp 5'
Search 100 bp 3'