Canonical Allele Identifier: CA1274240008
Gene: LINC01104 HGNC NCBI

Linked Data

dbSNP Id: rs1694219975

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100219122A>C , CM000664.2:g.100219122A>C GRCh38
NC_000002.11:g.100835584A>C , CM000664.1:g.100835584A>C GRCh37
NC_000002.10:g.100202016A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_103730.1:n.567+10302A>C