Canonical Allele Identifier: CA1230642205
Gene: LINC02774 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.244013122G>C , CM000663.2:g.244013122G>C GRCh38
NC_000001.10:g.244176424G>C , CM000663.1:g.244176424G>C GRCh37
NC_000001.9:g.242243047G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033883.1:n.750+2202G>C