Canonical Allele Identifier: CA2700063905
Gene: LINC01104 HGNC NCBI

Linked Data

dbSNP Id: rs2105672774

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100219083G>A , CM000664.2:g.100219083G>A GRCh38
NC_000002.11:g.100835545G>A , CM000664.1:g.100835545G>A GRCh37
NC_000002.10:g.100201977G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_103730.1:n.567+10263G>A