Canonical Allele Identifier: CA1576425886
Gene: LINC02208 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.118365840C= , CM000667.2:g.118365840C= GRCh38
NC_000005.9:g.117701535C= , CM000667.1:g.117701535C= GRCh37
NC_000005.8:g.117729434C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104610.1:n.2658-14333G=