Canonical Allele Identifier: CA1822904786
Gene: LINC02055 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.136837691A= , CM000670.2:g.136837691A= GRCh38
NC_000008.10:g.137849934A= , CM000670.1:g.137849934A= GRCh37
NC_000008.9:g.137919116A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_147196.1:n.443+40321A=