Canonical Allele Identifier: CA1034234460
Gene: LINC01104 HGNC NCBI

Linked Data

dbSNP Id: rs548435664

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100219094C>A , CM000664.2:g.100219094C>A GRCh38
NC_000002.11:g.100835556C>A , CM000664.1:g.100835556C>A GRCh37
NC_000002.10:g.100201988C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_103730.1:n.567+10274C>A