Canonical Allele Identifier: CA1274240152
Gene: LINC01104 HGNC NCBI

Linked Data

dbSNP Id: rs1694222429

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100219284C>T , CM000664.2:g.100219284C>T GRCh38
NC_000002.11:g.100835746C>T , CM000664.1:g.100835746C>T GRCh37
NC_000002.10:g.100202178C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_103730.1:n.567+10464C>T