Canonical Allele Identifier: CA1274240089
Gene: LINC01104 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100219226T= , CM000664.2:g.100219226T= GRCh38
NC_000002.11:g.100835688T= , CM000664.1:g.100835688T= GRCh37
NC_000002.10:g.100202120T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_103730.1:n.567+10406T=