Canonical Allele Identifier: CA1119097426
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816086617

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128529787A>G , CM000670.2:g.128529787A>G GRCh38
NC_000008.10:g.129542033A>G , CM000670.1:g.129542033A>G GRCh37
NC_000008.9:g.129611215A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+31283T>C