Canonical Allele Identifier: CA185876353
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1008640420
MyVariant Identifiers: chr8:g.129559200A>C (hg19) chr8:g.128546954A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128546954A>C , CM000670.2:g.128546954A>C GRCh38
NC_000008.10:g.129559200A>C , CM000670.1:g.129559200A>C GRCh37
NC_000008.9:g.129628382A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+14116T>G
Search 100 bp 5'
Search 100 bp 3'