Canonical Allele Identifier: CA1274236903
Gene: LINC01104 HGNC NCBI

Linked Data

dbSNP Id: rs1160542

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100215693G>C , CM000664.2:g.100215693G>C GRCh38
NC_000002.11:g.100832155G>C , CM000664.1:g.100832155G>C GRCh37
NC_000002.10:g.100198587G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_103730.1:n.567+6873G>C