ClinGen Allele Registry
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Canonical Allele Identifier:
CA15331198
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr4:g.99093654A>G
GRCh37
chr4:g.100014805A>G
Linked Data - Sequence & Population
gnomAD v2:
4:100014805 A / G
gnomAD v3:
4:99093654 A / G
gnomAD v4:
chr4-99093654-A-G
Joint Max Group AF
0.83725416 (EAS)
Genomes Max Group AF
0.83725416 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2602836
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.99093654A>G , CM000666.2:g.99093654A>G
GRCh38
NC_000004.11:g.100014805A>G , CM000666.1:g.100014805A>G
GRCh37
NC_000004.10:g.100233828A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_037884.1:n.428+4370A>G
Search 100 bp 5'
Search 100 bp 3'