Canonical Allele Identifier: CA1597487429
Gene: LINC02143 HGNC NCBI
LINC03000 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.164462274G= , CM000667.2:g.164462274G= GRCh38
NC_000005.9:g.163889280G= , CM000667.1:g.163889280G= GRCh37
NC_000005.8:g.163821858G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_105064.1:n.120+2525C= (LINC02143)
XR_001742489.1:n.585+108050G= (LINC03000)