ClinGen Allele Registry
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Canonical Allele Identifier:
CA12186531
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.30066107C>A
GRCh37
chr6:g.30033884C>A
Linked Data - Sequence & Population
gnomAD v2:
6:30033884 C / A
gnomAD v3:
6:30066107 C / A
gnomAD v4:
chr6-30066107-C-A
Joint Max Group AF
0.23603001 (EAS)
Genomes Max Group AF
0.23603001 (EAS)
Linked Data - NCBI & NCI
dbSNP:
3807031
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.30066107C>A , CM000668.2:g.30066107C>A
GRCh38
NC_000006.11:g.30033884C>A , CM000668.1:g.30033884C>A
GRCh37
NC_000006.10:g.30141863C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'