ClinGen Allele Registry
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Canonical Allele Identifier:
CA11904439
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.30066591A>C
GRCh37
chr4:g.30068213A>C
Linked Data - Sequence & Population
gnomAD v2:
4:30068213 A / C
gnomAD v3:
4:30066591 A / C
gnomAD v4:
chr4-30066591-A-C
Joint Max Group AF
0.49033601 (AFR)
Genomes Max Group AF
0.49033601 (AFR)
Linked Data - NCBI & NCI
dbSNP:
6818288
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.30066591A>C , CM000666.2:g.30066591A>C
GRCh38
NC_000004.11:g.30068213A>C , CM000666.1:g.30068213A>C
GRCh37
NC_000004.10:g.29677311A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'