ClinGen Allele Registry
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Canonical Allele Identifier:
CA95195627
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.33623080G>T
GRCh37
chr4:g.33624702G>T
Linked Data - Sequence & Population
gnomAD v2:
4:33624702 G / T
gnomAD v3:
4:33623080 G / T
gnomAD v4:
chr4-33623080-G-T
Joint Max Group AF
0.29369717 (AFR)
Genomes Max Group AF
0.29369717 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10517287
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.33623080G>T , CM000666.2:g.33623080G>T
GRCh38
NC_000004.11:g.33624702G>T , CM000666.1:g.33624702G>T
GRCh37
NC_000004.10:g.33301097G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'