Canonical Allele Identifier: CA1822904794
Gene: LINC02055 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.136837713T= , CM000670.2:g.136837713T= GRCh38
NC_000008.10:g.137849956T= , CM000670.1:g.137849956T= GRCh37
NC_000008.9:g.137919138T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_147196.1:n.443+40343T=