ClinGen Allele Registry
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Canonical Allele Identifier:
CA102238635
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.94449654G>A
GRCh37
chr4:g.95370805G>A
Linked Data - Sequence & Population
gnomAD v2:
4:95370805 G / A
gnomAD v3:
4:94449654 G / A
gnomAD v4:
chr4-94449654-G-A
Joint Max Group AF
0.43708897 (NFE)
Genomes Max Group AF
0.43708897 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2433320
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.94449654G>A , CM000666.2:g.94449654G>A
GRCh38
NC_000004.11:g.95370805G>A , CM000666.1:g.95370805G>A
GRCh37
NC_000004.10:g.95589828G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'