ClinGen Allele Registry
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Canonical Allele Identifier:
CA14961323
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr22:g.45034435C>G
GRCh37
chr22:g.45430316C>G
Linked Data - Sequence & Population
gnomAD v2:
22:45430316 C / G
gnomAD v3:
22:45034435 C / G
gnomAD v4:
chr22-45034435-C-G
Joint Max Group AF
0.32301276 (EAS)
Genomes Max Group AF
0.32301276 (EAS)
Linked Data - NCBI & NCI
dbSNP:
6007413
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.45034435C>G , CM000684.2:g.45034435C>G
GRCh38
NC_000022.10:g.45430316C>G , CM000684.1:g.45430316C>G
GRCh37
NC_000022.9:g.43808980C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'