Canonical Allele Identifier: CA2604623181
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs904910736

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128530183C>T , CM000670.2:g.128530183C>T GRCh38
NC_000008.10:g.129542429C>T , CM000670.1:g.129542429C>T GRCh37
NC_000008.9:g.129611611C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+30887G>A