ClinGen Allele Registry
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Canonical Allele Identifier:
CA12219129
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.166960059T>G
GRCh37
chr6:g.167373547T>G
Linked Data - Sequence & Population
gnomAD v2:
6:167373547 T / G
gnomAD v3:
6:166960059 T / G
gnomAD v4:
chr6-166960059-T-G
Joint Max Group AF
0.72533169 (AFR)
Genomes Max Group AF
0.72533169 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1819333
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.166960059T>G , CM000668.2:g.166960059T>G
GRCh38
NC_000006.11:g.167373547T>G , CM000668.1:g.167373547T>G
GRCh37
NC_000006.10:g.167293537T>G
NCBI36
NG_016280.1:g.1531A>C
NG_016280.2:g.1531A>C
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