ClinGen Allele Registry
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Canonical Allele Identifier:
CA11828710
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.46125050C>T
GRCh37
chr4:g.46127067C>T
Linked Data - Sequence & Population
gnomAD v2:
4:46127067 C / T
gnomAD v3:
4:46125050 C / T
gnomAD v4:
chr4-46125050-C-T
Joint Max Group AF
0.7470619 (AFR)
Genomes Max Group AF
0.7470619 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7654165
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.46125050C>T , CM000666.2:g.46125050C>T
GRCh38
NC_000004.11:g.46127067C>T , CM000666.1:g.46127067C>T
GRCh37
NC_000004.10:g.45821824C>T
NCBI36
NG_046964.1:g.4016G>A
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