ClinGen Allele Registry
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Canonical Allele Identifier:
CA14703628
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr19:g.44952331T>C
GRCh37
chr19:g.45455588T>C
Linked Data - Sequence & Population
gnomAD v2:
19:45455588 T / C
gnomAD v3:
19:44952331 T / C
gnomAD v4:
chr19-44952331-T-C
Joint Max Group AF
0.32140309 (SAS)
Genomes Max Group AF
0.32140309 (SAS)
Linked Data - NCBI & NCI
dbSNP:
10413089
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.44952331T>C , CM000681.2:g.44952331T>C
GRCh38
NC_000019.9:g.45455588T>C , CM000681.1:g.45455588T>C
GRCh37
NC_000019.8:g.50147428T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'