ClinGen Allele Registry
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Canonical Allele Identifier:
CA313510480
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr20:g.34141638T>G
GRCh37
chr20:g.32729444T>G
Linked Data - Sequence & Population
gnomAD v2:
20:32729444 T / G
gnomAD v3:
20:34141638 T / G
gnomAD v4:
chr20-34141638-T-G
Joint Max Group AF
0.84031121 (AFR)
Genomes Max Group AF
0.84031121 (AFR)
Linked Data - NCBI & NCI
dbSNP:
4911414
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.34141638T>G , CM000682.2:g.34141638T>G
GRCh38
NC_000020.10:g.32729444T>G , CM000682.1:g.32729444T>G
GRCh37
NC_000020.9:g.32193105T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'