ClinGen Allele Registry
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Canonical Allele Identifier:
CA11386815
Gene:
Linked Data
ClinVar RCV:
RCV001522189
RCV001709717
ClinVar Variation:
1170126
dbSNP:
5393
gnomAD v2:
3:170744920 T / G
gnomAD v3:
3:171027131 T / G
gnomAD v4:
chr3-171027131-T-G
Joint Max Group AF
0.46036717 (AFR)
Genomes Max Group AF
0.46036717 (AFR)
MyVariant.info:
GRCh38
chr3:g.171027131T>G
GRCh37
chr3:g.170744920T>G
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.171027131T>G , CM000665.2:g.171027131T>G
GRCh38
NC_000003.11:g.170744920T>G , CM000665.1:g.170744920T>G
GRCh37
NC_000003.10:g.172227614T>G
NCBI36
NG_008108.1:g.4849A>C
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