Canonical Allele Identifier: CA12135045
Gene: LINC03000 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.164297275A>G , CM000667.2:g.164297275A>G GRCh38
NC_000005.9:g.163724281A>G , CM000667.1:g.163724281A>G GRCh37
NC_000005.8:g.163656859A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742489.1:n.501+79A>G