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Canonical Allele Identifier:
CA104083522
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.110784612T>C
GRCh37
chr4:g.111705768T>C
Linked Data - Sequence & Population
gnomAD v2:
4:111705768 T / C
gnomAD v3:
4:110784612 T / C
gnomAD v4:
chr4-110784612-T-C
Joint Max Group AF
0.48735816 (EAS)
Genomes Max Group AF
0.48735816 (EAS)
Linked Data - NCBI & NCI
dbSNP:
6817105
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.110784612T>C , CM000666.2:g.110784612T>C
GRCh38
NC_000004.11:g.111705768T>C , CM000666.1:g.111705768T>C
GRCh37
NC_000004.10:g.111925217T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'