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Canonical Allele Identifier:
CA14662782
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.45655255T>G
GRCh37
chr19:g.46158513T>G
Linked Data - Sequence & Population
gnomAD v2:
19:46158513 T / G
gnomAD v3:
19:45655255 T / G
gnomAD v4:
chr19-45655255-T-G
Joint Max Group AF
0.45877001 (EAS)
Genomes Max Group AF
0.45877001 (EAS)
Linked Data - NCBI & NCI
dbSNP:
8108269
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.45655255T>G , CM000681.2:g.45655255T>G
GRCh38
NC_000019.9:g.46158513T>G , CM000681.1:g.46158513T>G
GRCh37
NC_000019.8:g.50850353T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'