Canonical Allele Identifier: CA1576425890
Gene: LINC02208 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.118365843T= , CM000667.2:g.118365843T= GRCh38
NC_000005.9:g.117701538T= , CM000667.1:g.117701538T= GRCh37
NC_000005.8:g.117729437T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104610.1:n.2658-14336A=