Canonical Allele Identifier: CA2782164960
Gene: LINC00824 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128529751G>C , CM000670.2:g.128529751G>C GRCh38
NC_000008.10:g.129541997G>C , CM000670.1:g.129541997G>C GRCh37
NC_000008.9:g.129611179G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+31319C>G