Canonical Allele Identifier: CA1274240161
Gene: LINC01104 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100219295G= , CM000664.2:g.100219295G= GRCh38
NC_000002.11:g.100835757G= , CM000664.1:g.100835757G= GRCh37
NC_000002.10:g.100202189G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_103730.1:n.567+10475G=