ClinGen Allele Registry
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Canonical Allele Identifier:
CA12231316
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr6:g.31578718G>C
GRCh37
chr6:g.31546495G>C
Linked Data - Sequence & Population
gnomAD v2:
6:31546495 G / C
gnomAD v3:
6:31578718 G / C
gnomAD v4:
chr6-31578718-G-C
Joint Max Group AF
0.05559005 (SAS)
Genomes Max Group AF
0.05559005 (SAS)
Linked Data - NCBI & NCI
dbSNP:
3093668
2113413030
2113413039
2113413063
2113413071
2113413080
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.31578718G>C , CM000668.2:g.31578718G>C
GRCh38
NC_000006.11:g.31546495G>C , CM000668.1:g.31546495G>C
GRCh37
NC_000006.10:g.31654474G>C
NCBI36
NG_007462.1:g.8146G>C
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