ClinGen Allele Registry
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Canonical Allele Identifier:
CA11379306
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr3:g.136207780G>T
GRCh37
chr3:g.135926622G>T
Linked Data - Sequence & Population
gnomAD v2:
3:135926622 G / T
gnomAD v3:
3:136207780 G / T
gnomAD v4:
chr3-136207780-G-T
Joint Max Group AF
0.8444891 (EAS)
Genomes Max Group AF
0.8444891 (EAS)
Linked Data - NCBI & NCI
dbSNP:
645040
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.136207780G>T , CM000665.2:g.136207780G>T
GRCh38
NC_000003.11:g.135926622G>T , CM000665.1:g.135926622G>T
GRCh37
NC_000003.10:g.137409312G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'