ClinGen Allele Registry
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Canonical Allele Identifier:
CA13222962
Gene: LINC02640
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.68238298A>C
GRCh37
chr10:g.69998055A>C
Linked Data - Sequence & Population
gnomAD v2:
10:69998055 A / C
gnomAD v3:
10:68238298 A / C
gnomAD v4:
chr10-68238298-A-C
Joint Max Group AF
0.75169708 (NFE)
Genomes Max Group AF
0.75169708 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1900005
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.68238298A>C , CM000672.2:g.68238298A>C
GRCh38
NC_000010.10:g.69998055A>C , CM000672.1:g.69998055A>C
GRCh37
NC_000010.9:g.69668061A>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_001747481.1:n.104-667T>G
Search 100 bp 5'
Search 100 bp 3'