Canonical Allele Identifier: CA1818921432
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816092471

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128530135A>C , CM000670.2:g.128530135A>C GRCh38
NC_000008.10:g.129542381A>C , CM000670.1:g.129542381A>C GRCh37
NC_000008.9:g.129611563A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+30935T>G