ClinGen Allele Registry
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Canonical Allele Identifier:
CA11460685
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr3:g.172449471T>A
GRCh37
chr3:g.172167261T>A
Linked Data - Sequence & Population
gnomAD v2:
3:172167261 T / A
gnomAD v3:
3:172449471 T / A
gnomAD v4:
chr3-172449471-T-A
Joint Max Group AF
0.43075188 (EAS)
Genomes Max Group AF
0.43075188 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2922126
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.172449471T>A , CM000665.2:g.172449471T>A
GRCh38
NC_000003.11:g.172167261T>A , CM000665.1:g.172167261T>A
GRCh37
NC_000003.10:g.173649955T>A
NCBI36
NG_021159.1:g.3986A>T
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