Canonical Allele Identifier: CA1763291169
Gene: LINC03022 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10477271T= , CM000670.2:g.10477271T= GRCh38
NC_000008.10:g.10334781T= , CM000670.1:g.10334781T= GRCh37
NC_000008.9:g.10372191T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120604.1:n.216T=