ClinGen Allele Registry
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Canonical Allele Identifier:
CA16571427
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.33829949A>C
GRCh37
chr19:g.34320854A>C
Linked Data - Sequence & Population
gnomAD v2:
19:34320854 A / C
gnomAD v3:
19:33829949 A / C
gnomAD v4:
chr19-33829949-A-C
Joint Max Group AF
0.490295 (AMR)
Genomes Max Group AF
0.490295 (AMR)
Linked Data - NCBI & NCI
dbSNP:
2546057
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.33829949A>C , CM000681.2:g.33829949A>C
GRCh38
NC_000019.9:g.34320854A>C , CM000681.1:g.34320854A>C
GRCh37
NC_000019.8:g.39012694A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'