Canonical Allele Identifier: CA1534016627
Gene: LINC02211 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.25420023C= , CM000667.2:g.25420023C= GRCh38
NC_000005.9:g.25420132C= , CM000667.1:g.25420132C= GRCh37
NC_000005.8:g.25455889C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011514196.1:c.*59+63925C= XP_011512498.1:n.*59+63925C=