Canonical Allele Identifier: CA185874207
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs34537239
gnomAD v2: 8-129542349-GA-G
gnomAD v3: 8-128530103-GA-G
gnomAD v4: 8-128530103-GA-G
MyVariant Identifiers: chr8:g.129542350del (hg19) chr8:g.128530104del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128530106del , CM000670.2:g.128530106del GRCh38
NC_000008.10:g.129542352del , CM000670.1:g.129542352del GRCh37
NC_000008.9:g.129611534del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+30966del
Search 100 bp 5'
Search 100 bp 3'