Canonical Allele Identifier: CA185876394
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1053028233
gnomAD v3: 8-128547237-A-T
gnomAD v4: 8-128547237-A-T
MyVariant Identifiers: chr8:g.129559483A>T (hg19) chr8:g.128547237A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547237A>T , CM000670.2:g.128547237A>T GRCh38
NC_000008.10:g.129559483A>T , CM000670.1:g.129559483A>T GRCh37
NC_000008.9:g.129628665A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+13833T>A
Search 100 bp 5'
Search 100 bp 3'