ClinGen Allele Registry
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Canonical Allele Identifier:
CA110082061
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.163323901T>A
GRCh37
chr4:g.164245053T>A
Linked Data - Sequence & Population
gnomAD v2:
4:164245053 T / A
gnomAD v3:
4:163323901 T / A
gnomAD v4:
chr4-163323901-T-A
Joint Max Group AF
0.60813877 (NFE)
Genomes Max Group AF
0.60813877 (NFE)
Linked Data - NCBI & NCI
dbSNP:
4057797
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.163323901T>A , CM000666.2:g.163323901T>A
GRCh38
NC_000004.11:g.164245053T>A , CM000666.1:g.164245053T>A
GRCh37
NC_000004.10:g.164464503T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'