ClinGen Allele Registry
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Canonical Allele Identifier:
CA11909542
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr4:g.111690594T>C
GRCh37
chr4:g.112611750T>C
Linked Data - Sequence & Population
gnomAD v2:
4:112611750 T / C
gnomAD v3:
4:111690594 T / C
gnomAD v4:
chr4-111690594-T-C
Joint Max Group AF
0.45393599 (SAS)
Genomes Max Group AF
0.45393599 (SAS)
Linked Data - NCBI & NCI
dbSNP:
10034228
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.111690594T>C , CM000666.2:g.111690594T>C
GRCh38
NC_000004.11:g.112611750T>C , CM000666.1:g.112611750T>C
GRCh37
NC_000004.10:g.112831199T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'