ClinGen Allele Registry
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Canonical Allele Identifier:
CA14703689
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.45305950T>C
GRCh37
chr19:g.45809208T>C
Linked Data - Sequence & Population
gnomAD v2:
19:45809208 T / C
gnomAD v3:
19:45305950 T / C
gnomAD v4:
chr19-45305950-T-C
Joint Max Group AF
0.49215255 (AFR)
Genomes Max Group AF
0.49215255 (AFR)
Linked Data - NCBI & NCI
dbSNP:
8111989
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.45305950T>C , CM000681.2:g.45305950T>C
GRCh38
NC_000019.9:g.45809208T>C , CM000681.1:g.45809208T>C
GRCh37
NC_000019.8:g.50501048T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'