Canonical Allele Identifier: CA2312765835
Gene: LINC01899 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.71771837G= , CM000680.2:g.71771837G= GRCh38
NC_000018.9:g.69439073G= , CM000680.1:g.69439073G= GRCh37
NC_000018.8:g.67590053G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126324.1:n.37+10353C=