Canonical Allele Identifier: CA2589255244
Gene: LINC00278 HGNC NCBI

Linked Data

gnomAD v3: Y-3004605-C-T
gnomAD v4: Y-3004605-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.3004605C>T , CM000686.2:g.3004605C>T GRCh38
NC_000024.9:g.2872646C>T , CM000686.1:g.2872646C>T GRCh37
NC_000024.8:g.2932646C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_046502.1:n.222+1388C>T