Canonical Allele Identifier: CA185876396
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1020433614
gnomAD v3: 8-128547264-C-T
gnomAD v4: 8-128547264-C-T
MyVariant Identifiers: chr8:g.129559510C>T (hg19) chr8:g.128547264C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128547264C>T , CM000670.2:g.128547264C>T GRCh38
NC_000008.10:g.129559510C>T , CM000670.1:g.129559510C>T GRCh37
NC_000008.9:g.129628692C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+13806G>A
Search 100 bp 5'
Search 100 bp 3'