Canonical Allele Identifier: CA1034234494
Gene: LINC01104 HGNC NCBI

Linked Data

dbSNP Id: rs1694221139

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100219191C>T , CM000664.2:g.100219191C>T GRCh38
NC_000002.11:g.100835653C>T , CM000664.1:g.100835653C>T GRCh37
NC_000002.10:g.100202085C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_103730.1:n.567+10371C>T