ClinGen Allele Registry
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Canonical Allele Identifier:
CA99599175
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.81228852T>G
GRCh37
chr4:g.82150006T>G
Linked Data - Sequence & Population
gnomAD v2:
4:82150006 T / G
gnomAD v3:
4:81228852 T / G
gnomAD v4:
chr4-81228852-T-G
Joint Max Group AF
0.65266853 (AFR)
Genomes Max Group AF
0.65266853 (AFR)
Linked Data - NCBI & NCI
dbSNP:
788867
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.81228852T>G , CM000666.2:g.81228852T>G
GRCh38
NC_000004.11:g.82150006T>G , CM000666.1:g.82150006T>G
GRCh37
NC_000004.10:g.82369030T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'