ClinGen Allele Registry
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Canonical Allele Identifier:
CA16163120
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.157080986T>C
GRCh37
chr3:g.156798775T>C
Linked Data - Sequence & Population
gnomAD v2:
3:156798775 T / C
gnomAD v3:
3:157080986 T / C
gnomAD v4:
chr3-157080986-T-C
Joint Max Group AF
0.48718006 (EAS)
Genomes Max Group AF
0.48718006 (EAS)
Linked Data - NCBI & NCI
dbSNP:
900400
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.157080986T>C , CM000665.2:g.157080986T>C
GRCh38
NC_000003.11:g.156798775T>C , CM000665.1:g.156798775T>C
GRCh37
NC_000003.10:g.158281469T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'