Canonical Allele Identifier: CA1576425861
Gene: LINC02208 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.118365791A= , CM000667.2:g.118365791A= GRCh38
NC_000005.9:g.117701486A= , CM000667.1:g.117701486A= GRCh37
NC_000005.8:g.117729385A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104610.1:n.2658-14284T=