Canonical Allele Identifier: CA1138672797
Gene: LINC00278 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.3019783A>G , CM000686.2:g.3019783A>G GRCh38
NC_000024.9:g.2887824A>G , CM000686.1:g.2887824A>G GRCh37
NC_000024.8:g.2947824A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046502.1:n.222+16566A>G