Canonical Allele Identifier: CA1818909507
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1586657471

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547130A>C , CM000670.2:g.128547130A>C GRCh38
NC_000008.10:g.129559376A>C , CM000670.1:g.129559376A>C GRCh37
NC_000008.9:g.129628558A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+13940T>G