ClinGen Allele Registry
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Canonical Allele Identifier:
CA12266089
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.31605179A>C
GRCh37
chr6:g.31572956A>C
Linked Data - Sequence & Population
gnomAD v2:
6:31572956 A / C
gnomAD v3:
6:31605179 A / C
gnomAD v4:
chr6-31605179-A-C
Joint Max Group AF
0.44990359 (MID)
Genomes Max Group AF
0.44223583 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2844479
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.31605179A>C , CM000668.2:g.31605179A>C
GRCh38
NC_000006.11:g.31572956A>C , CM000668.1:g.31572956A>C
GRCh37
NC_000006.10:g.31680935A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'