Canonical Allele Identifier: CA1597811818
Gene: LINC03000 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.165119891A= , CM000667.2:g.165119891A= GRCh38
NC_000005.9:g.164546897A= , CM000667.1:g.164546897A= GRCh37
NC_000005.8:g.164479475A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941179.1:n.357-51487A=