ClinGen Allele Registry
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Canonical Allele Identifier:
CA11673276
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.188199757T>C
GRCh37
chr4:g.189120911T>C
Linked Data - Sequence & Population
gnomAD v2:
4:189120911 T / C
gnomAD v3:
4:188199757 T / C
gnomAD v4:
chr4-188199757-T-C
Joint Max Group AF
0.96664121 (EAS)
Genomes Max Group AF
0.96664121 (EAS)
Linked Data - NCBI & NCI
dbSNP:
6857559
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.188199757T>C , CM000666.2:g.188199757T>C
GRCh38
NC_000004.11:g.189120911T>C , CM000666.1:g.189120911T>C
GRCh37
NC_000004.10:g.189357905T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'