ClinGen Allele Registry
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Canonical Allele Identifier:
CA12266080
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr6:g.31574531T>C
GRCh37
chr6:g.31542308T>C
Linked Data - Sequence & Population
gnomAD v2:
6:31542308 T / C
gnomAD v3:
6:31574531 T / C
gnomAD v4:
chr6-31574531-T-C
Joint Max Group AF
0.31085855 (SAS)
Genomes Max Group AF
0.31085855 (SAS)
Linked Data - NCBI & NCI
dbSNP:
1799964
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.31574531T>C , CM000668.2:g.31574531T>C
GRCh38
NC_000006.11:g.31542308T>C , CM000668.1:g.31542308T>C
GRCh37
NC_000006.10:g.31650287T>C
NCBI36
NG_007462.1:g.3959T>C
NG_012010.1:g.7433T>C
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