Canonical Allele Identifier: CA1818921160
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1586652008

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128529805A>C , CM000670.2:g.128529805A>C GRCh38
NC_000008.10:g.129542051A>C , CM000670.1:g.129542051A>C GRCh37
NC_000008.9:g.129611233A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+31265T>G