ClinGen Allele Registry
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Canonical Allele Identifier:
CA16196665
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.110796911G>A
GRCh37
chr4:g.111718067G>A
Linked Data - Sequence & Population
gnomAD v2:
4:111718067 G / A
gnomAD v3:
4:110796911 G / A
gnomAD v4:
chr4-110796911-G-A
Joint Max Group AF
0.76484828 (NFE)
Genomes Max Group AF
0.7648345 (NFE)
Exomes Max Group AF
0.34157938 (AFR)
Linked Data - NCBI & NCI
dbSNP:
6843082
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.110796911G>A , CM000666.2:g.110796911G>A
GRCh38
NC_000004.11:g.111718067G>A , CM000666.1:g.111718067G>A
GRCh37
NC_000004.10:g.111937516G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'