Canonical Allele Identifier: CA53081665
Gene: LINC01104 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10865035

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100219272A>G , CM000664.2:g.100219272A>G GRCh38
NC_000002.11:g.100835734A>G , CM000664.1:g.100835734A>G GRCh37
NC_000002.10:g.100202166A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_103730.1:n.567+10452A>G