ClinGen Allele Registry
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Canonical Allele Identifier:
CA12187968
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.32184610A>T
GRCh37
chr6:g.32152387A>T
Linked Data - Sequence & Population
gnomAD v2:
6:32152387 A / T
gnomAD v3:
6:32184610 A / T
gnomAD v4:
chr6-32184610-A-T
Joint Max Group AF
0.33716857 (MID)
Genomes Max Group AF
0.29940683 (AMR)
Exomes Max Group AF
0.33820724 (MID)
Linked Data - NCBI & NCI
dbSNP:
1800624
2113350873
2113350945
2113350967
2113351032
2113351050
2113351080
2113351092
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.32184610A>T , CM000668.2:g.32184610A>T
GRCh38
NC_000006.11:g.32152387A>T , CM000668.1:g.32152387A>T
GRCh37
NC_000006.10:g.32260365A>T
NCBI36
NG_029868.1:g.4713T>A
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