ClinGen Allele Registry
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Canonical Allele Identifier:
CA16194721
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.100885375C>G
GRCh37
chr4:g.101806532C>G
Linked Data - Sequence & Population
gnomAD v2:
4:101806532 C / G
gnomAD v3:
4:100885375 C / G
gnomAD v4:
chr4-100885375-C-G
Joint Max Group AF
0.24561817 (NFE)
Genomes Max Group AF
0.24561817 (NFE)
Linked Data - NCBI & NCI
dbSNP:
13107740
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.100885375C>G , CM000666.2:g.100885375C>G
GRCh38
NC_000004.11:g.101806532C>G , CM000666.1:g.101806532C>G
GRCh37
NC_000004.10:g.102025555C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'