Canonical Allele Identifier: CA1034234497
Gene: LINC01104 HGNC NCBI

Linked Data

dbSNP Id: rs1694221167

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100219192C>A , CM000664.2:g.100219192C>A GRCh38
NC_000002.11:g.100835654C>A , CM000664.1:g.100835654C>A GRCh37
NC_000002.10:g.100202086C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_103730.1:n.567+10372C>A