Canonical Allele Identifier: CA1822904782
Gene: LINC02055 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.136837680T= , CM000670.2:g.136837680T= GRCh38
NC_000008.10:g.137849923T= , CM000670.1:g.137849923T= GRCh37
NC_000008.9:g.137919105T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_147196.1:n.443+40310T=