Canonical Allele Identifier: CA2581474382
Gene: LINC02211 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.25419980G>C , CM000667.2:g.25419980G>C GRCh38
NC_000005.9:g.25420089G>C , CM000667.1:g.25420089G>C GRCh37
NC_000005.8:g.25455846G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011514196.1:c.*59+63882G>C XP_011512498.1:n.*59+63882G>C