Canonical Allele Identifier: CA185874217
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs1044840641
gnomAD v3: 8-128530160-C-T
gnomAD v4: 8-128530160-C-T
MyVariant Identifiers: chr8:g.129542406C>T (hg19) chr8:g.128530160C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128530160C>T , CM000670.2:g.128530160C>T GRCh38
NC_000008.10:g.129542406C>T , CM000670.1:g.129542406C>T GRCh37
NC_000008.9:g.129611588C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+30910G>A
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