Canonical Allele Identifier: CA754154385
Gene: LINC01104 HGNC NCBI

Linked Data

dbSNP Id: rs1414103941

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100219144T>C , CM000664.2:g.100219144T>C GRCh38
NC_000002.11:g.100835606T>C , CM000664.1:g.100835606T>C GRCh37
NC_000002.10:g.100202038T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_103730.1:n.567+10324T>C