ClinGen Allele Registry
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Canonical Allele Identifier:
CA12219124
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.166957622T>C
GRCh37
chr6:g.167371110T>C
Linked Data - Sequence & Population
gnomAD v2:
6:167371110 T / C
gnomAD v3:
6:166957622 T / C
gnomAD v4:
chr6-166957622-T-C
Joint Max Group AF
0.72985083 (AFR)
Genomes Max Group AF
0.72985083 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2149085
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.166957622T>C , CM000668.2:g.166957622T>C
GRCh38
NC_000006.11:g.167371110T>C , CM000668.1:g.167371110T>C
GRCh37
NC_000006.10:g.167291100T>C
NCBI36
NG_016280.1:g.3968A>G
NG_016280.2:g.3968A>G
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