Canonical Allele Identifier: CA185876337
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs114402349
gnomAD v2: 8-129559076-T-G
gnomAD v3: 8-128546830-T-G
gnomAD v4: 8-128546830-T-G
MyVariant Identifiers: chr8:g.129559076T>G (hg19) chr8:g.128546830T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128546830T>G , CM000670.2:g.128546830T>G GRCh38
NC_000008.10:g.129559076T>G , CM000670.1:g.129559076T>G GRCh37
NC_000008.9:g.129628258T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+14240A>C
Search 100 bp 5'
Search 100 bp 3'