Canonical Allele Identifier: CA1274239981
Gene: LINC01104 HGNC NCBI

Linked Data

dbSNP Id: rs1694219538

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100219085G>A , CM000664.2:g.100219085G>A GRCh38
NC_000002.11:g.100835547G>A , CM000664.1:g.100835547G>A GRCh37
NC_000002.10:g.100201979G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_103730.1:n.567+10265G>A