Canonical Allele Identifier: CA2782164961
Gene: LINC00824 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128529770C>T , CM000670.2:g.128529770C>T GRCh38
NC_000008.10:g.129542016C>T , CM000670.1:g.129542016C>T GRCh37
NC_000008.9:g.129611198C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+31300G>A