Canonical Allele Identifier: CA53081671
Gene: LINC01104 HGNC NCBI

Linked Data

dbSNP Id: rs1023085397

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100219327A>G , CM000664.2:g.100219327A>G GRCh38
NC_000002.11:g.100835789A>G , CM000664.1:g.100835789A>G GRCh37
NC_000002.10:g.100202221A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_103730.1:n.567+10507A>G