Canonical Allele Identifier: CA2718147971
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1816086551

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128529773G>C , CM000670.2:g.128529773G>C GRCh38
NC_000008.10:g.129542019G>C , CM000670.1:g.129542019G>C GRCh37
NC_000008.9:g.129611201G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_121672.1:n.508+31297C>G