Canonical Allele Identifier: CA1597785325
Gene: LINC03000 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.165057942T= , CM000667.2:g.165057942T= GRCh38
NC_000005.9:g.164484948T= , CM000667.1:g.164484948T= GRCh37
NC_000005.8:g.164417526T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742489.1:n.2476T=
XR_941179.1:n.356+50530T=