Canonical Allele Identifier: CA1641905369
Gene: LINC02542 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.82084877T= , CM000668.2:g.82084877T= GRCh38
NC_000006.11:g.82794594T= , CM000668.1:g.82794594T= GRCh37
NC_000006.10:g.82851313T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_942730.1:n.135+878A=
XR_942732.1:n.135+878A=
XR_942733.1:n.135+878A=
NR_149135.1:n.207-12632A=
XR_001744231.1:n.1197+15773T=