Canonical Allele Identifier: CA1274230242
Gene: LINC01104 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100208905C= , CM000664.2:g.100208905C= GRCh38
NC_000002.11:g.100825367C= , CM000664.1:g.100825367C= GRCh37
NC_000002.10:g.100191799C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_103730.1:n.567+85C=