ClinGen Allele Registry
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Canonical Allele Identifier:
CA11776162
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr4:g.37062709G>T
GRCh37
chr4:g.37064331G>T
Linked Data - Sequence & Population
gnomAD v2:
4:37064331 G / T
gnomAD v3:
4:37062709 G / T
gnomAD v4:
chr4-37062709-G-T
Joint Max Group AF
0.43973252 (EAS)
Genomes Max Group AF
0.43973252 (EAS)
Linked Data - NCBI & NCI
dbSNP:
13117816
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.37062709G>T , CM000666.2:g.37062709G>T
GRCh38
NC_000004.11:g.37064331G>T , CM000666.1:g.37064331G>T
GRCh37
NC_000004.10:g.36740726G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'