Canonical Allele Identifier: CA847294136
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1302796295
MyVariant Identifiers: chr8:g.129542370G>T (hg19) chr8:g.128530124G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128530124G>T , CM000670.2:g.128530124G>T GRCh38
NC_000008.10:g.129542370G>T , CM000670.1:g.129542370G>T GRCh37
NC_000008.9:g.129611552G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+30946C>A
Search 100 bp 5'
Search 100 bp 3'