ClinGen Allele Registry
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Canonical Allele Identifier:
CA11427620
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr3:g.169763483C>G
GRCh37
chr3:g.169481271C>G
Linked Data - Sequence & Population
gnomAD v2:
3:169481271 C / G
gnomAD v3:
3:169763483 C / G
gnomAD v4:
chr3-169763483-C-G
Joint Max Group AF
0.66177414 (EAS)
Genomes Max Group AF
0.66177414 (EAS)
Linked Data - NCBI & NCI
dbSNP:
12696304
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.169763483C>G , CM000665.2:g.169763483C>G
GRCh38
NC_000003.11:g.169481271C>G , CM000665.1:g.169481271C>G
GRCh37
NC_000003.10:g.170963965C>G
NCBI36
NG_016363.1:g.6578G>C , LRG_347:g.6578G>C
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