Canonical Allele Identifier: CA1597487430
Gene: LINC02143 HGNC NCBI
LINC03000 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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