Canonical Allele Identifier: CA847304276
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1466433152

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547228T>C , CM000670.2:g.128547228T>C GRCh38
NC_000008.10:g.129559474T>C , CM000670.1:g.129559474T>C GRCh37
NC_000008.9:g.129628656T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+13842A>G