Canonical Allele Identifier: CA1119100850
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1307059786

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547094G>T , CM000670.2:g.128547094G>T GRCh38
NC_000008.10:g.129559340G>T , CM000670.1:g.129559340G>T GRCh37
NC_000008.9:g.129628522G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+13976C>A