Canonical Allele Identifier: CA1119097603
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816093372

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128530191T>C , CM000670.2:g.128530191T>C GRCh38
NC_000008.10:g.129542437T>C , CM000670.1:g.129542437T>C GRCh37
NC_000008.9:g.129611619T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+30879A>G