Canonical Allele Identifier: CA585113119
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1398273397

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128554869A>T , CM000670.2:g.128554869A>T GRCh38
NC_000008.10:g.129567115A>T , CM000670.1:g.129567115A>T GRCh37
NC_000008.9:g.129636297A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+6201T>A