Canonical Allele Identifier: CA13363082
Gene: LINC00841 HGNC NCBI

Linked Data

dbSNP Id: rs898549

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43963266C>T , CM000672.2:g.43963266C>T GRCh38
NC_000010.10:g.44458714C>T , CM000672.1:g.44458714C>T GRCh37
NC_000010.9:g.43778720C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_033846.1:n.605-2117C>T
NR_033846.2:n.613-2117C>T
NR_136147.1:n.397+7951C>T