Canonical Allele Identifier: CA1966943684
Gene: LINC02740 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.42225168G>T , CM000673.2:g.42225168G>T GRCh38
NC_000011.9:g.42246718G>T , CM000673.1:g.42246718G>T GRCh37
NC_000011.8:g.42203294G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038309.1:n.332+12925C>A