Canonical Allele Identifier: CA463032283
Gene: LINC00824 HGNC NCBI

Linked Data

dbSNP Id: rs951261868
gnomAD v2: 8-129542253-T-TA
gnomAD v3: 8-128530007-T-TA
gnomAD v4: 8-128530007-T-TA
MyVariant Identifiers: chr8:g.129542253_129542254insA (hg19) chr8:g.128530007_128530008insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128530007_128530008insA , CM000670.2:g.128530007_128530008insA GRCh38
NC_000008.10:g.129542253_129542254insA , CM000670.1:g.129542253_129542254insA GRCh37
NC_000008.9:g.129611435_129611436insA NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+31062_508+31063insT
Search 100 bp 5'
Search 100 bp 3'