Canonical Allele Identifier: CA1534016619
Gene: LINC02211 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.25420016T= , CM000667.2:g.25420016T= GRCh38
NC_000005.9:g.25420125T= , CM000667.1:g.25420125T= GRCh37
NC_000005.8:g.25455882T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011514196.1:c.*59+63918T= XP_011512498.1:n.*59+63918T=