ClinGen Allele Registry
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Canonical Allele Identifier:
CA117706959
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.40392626T>C
GRCh37
chr5:g.40392728T>C
Linked Data - Sequence & Population
gnomAD v2:
5:40392728 T / C
gnomAD v3:
5:40392626 T / C
gnomAD v4:
chr5-40392626-T-C
Joint Max Group AF
0.18597212 (AFR)
Genomes Max Group AF
0.18597212 (AFR)
Linked Data - NCBI & NCI
dbSNP:
4613763
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.40392626T>C , CM000667.2:g.40392626T>C
GRCh38
NC_000005.9:g.40392728T>C , CM000667.1:g.40392728T>C
GRCh37
NC_000005.8:g.40428485T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'