Canonical Allele Identifier: CA535050370
Gene: LINC01104 HGNC NCBI

Linked Data

dbSNP Id: rs1259284092

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100219227A>G , CM000664.2:g.100219227A>G GRCh38
NC_000002.11:g.100835689A>G , CM000664.1:g.100835689A>G GRCh37
NC_000002.10:g.100202121A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_103730.1:n.567+10407A>G