Canonical Allele Identifier: CA16348818
Gene: LINC00824 HGNC NCBI
dbSNP:
10098821
gnomAD v2:
8:129559228 C / T
gnomAD v3:
8:128546982 C / T
gnomAD v4:
chr8-128546982-C-T
Joint Max Group AF 0.11245722 (MID)
Genomes Max Group AF 0.10893835 (NFE)
MyVariant.info:
GRCh38 chr8:g.128546982C>T
GRCh37 chr8:g.129559228C>T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.128546982C>T , CM000670.2:g.128546982C>T GRCh38
NC_000008.10:g.129559228C>T , CM000670.1:g.129559228C>T GRCh37
NC_000008.9:g.129628410C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_121672.1:n.508+14088G>A
Search 100 bp 5'
Search 100 bp 3'