Canonical Allele Identifier: CA1119101975
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1398273397

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128554869A>G , CM000670.2:g.128554869A>G GRCh38
NC_000008.10:g.129567115A>G , CM000670.1:g.129567115A>G GRCh37
NC_000008.9:g.129636297A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+6201T>C