ClinGen Allele Registry
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Canonical Allele Identifier:
CA12230999
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.31372436T>A
GRCh37
chr6:g.31340213T>A
Linked Data - Sequence & Population
gnomAD v2:
6:31340213 T / A
gnomAD v3:
6:31372436 T / A
gnomAD v4:
chr6-31372436-T-A
Joint Max Group AF
0.69504036 (EAS)
Genomes Max Group AF
0.69504036 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2596439
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.31372436T>A , CM000668.2:g.31372436T>A
GRCh38
NC_000006.11:g.31340213T>A , CM000668.1:g.31340213T>A
GRCh37
NC_000006.10:g.31448192T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'