Canonical Allele Identifier: CA2580596634
Gene: LINC00824 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128546982C>G , CM000670.2:g.128546982C>G GRCh38
NC_000008.10:g.129559228C>G , CM000670.1:g.129559228C>G GRCh37
NC_000008.9:g.129628410C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+14088G>C