Canonical Allele Identifier: CA1119097541
Gene: LINC00824 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128530070A>T , CM000670.2:g.128530070A>T GRCh38
NC_000008.10:g.129542316A>T , CM000670.1:g.129542316A>T GRCh37
NC_000008.9:g.129611498A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+31000T>A