Canonical Allele Identifier: CA1034234502
Gene: LINC01104 HGNC NCBI

Linked Data

dbSNP Id: rs1694221564

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NR_103730.1:n.567+10406T>A