Canonical Allele Identifier: CA2718329841
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs2130602177

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128531628T>G , CM000670.2:g.128531628T>G GRCh38
NC_000008.10:g.129543874T>G , CM000670.1:g.129543874T>G GRCh37
NC_000008.9:g.129613056T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+29442A>C