ClinGen Allele Registry
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Canonical Allele Identifier:
CA15366648
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.166530081T>G
GRCh37
chr5:g.165957086T>G
Linked Data - Sequence & Population
gnomAD v2:
5:165957086 T / G
gnomAD v3:
5:166530081 T / G
gnomAD v4:
chr5-166530081-T-G
Joint Max Group AF
0.95962315 (NFE)
Genomes Max Group AF
0.95962315 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2122554
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.166530081T>G , CM000667.2:g.166530081T>G
GRCh38
NC_000005.9:g.165957086T>G , CM000667.1:g.165957086T>G
GRCh37
NC_000005.8:g.165889664T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'