Canonical Allele Identifier: CA3134682899
Gene: LINC02540 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.76556471G= , CM000668.2:g.76556471G= GRCh38
NC_000006.11:g.77266188G= , CM000668.1:g.77266188G= GRCh37
NC_000006.10:g.77322907G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_942696.1:n.393+29977C=
NR_149101.1:n.216+29977C=