Canonical Allele Identifier: CA1274240155
Gene: LINC01104 HGNC NCBI

Linked Data

dbSNP Id: rs1694222456

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100219287C>A , CM000664.2:g.100219287C>A GRCh38
NC_000002.11:g.100835749C>A , CM000664.1:g.100835749C>A GRCh37
NC_000002.10:g.100202181C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_103730.1:n.567+10467C>A