ClinGen Allele Registry
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Canonical Allele Identifier:
CA16162246
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.152834401C>T
GRCh37
chr3:g.152552190C>T
Linked Data - Sequence & Population
gnomAD v2:
3:152552190 C / T
gnomAD v3:
3:152834401 C / T
gnomAD v4:
chr3-152834401-C-T
Joint Max Group AF
0.66960649 (AFR)
Genomes Max Group AF
0.66960649 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1371097
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.152834401C>T , CM000665.2:g.152834401C>T
GRCh38
NC_000003.11:g.152552190C>T , CM000665.1:g.152552190C>T
GRCh37
NC_000003.10:g.154034880C>T
NCBI36
NG_032896.2:g.4455C>T
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