Canonical Allele Identifier: CA1818921229
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1586652041

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128529910T>C , CM000670.2:g.128529910T>C GRCh38
NC_000008.10:g.129542156T>C , CM000670.1:g.129542156T>C GRCh37
NC_000008.9:g.129611338T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+31160A>G