ClinGen Allele Registry
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Canonical Allele Identifier:
CA14634024
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.7670589G>C
GRCh37
chr19:g.7735475G>C
Linked Data - Sequence & Population
gnomAD v2:
19:7735475 G / C
gnomAD v3:
19:7670589 G / C
gnomAD v4:
chr19-7670589-G-C
Joint Max Group AF
0.5242397 (SAS)
Genomes Max Group AF
0.50249542 (AMR)
Exomes Max Group AF
0.52514489 (SAS)
Linked Data - NCBI & NCI
dbSNP:
3745369
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.7670589G>C , CM000681.2:g.7670589G>C
GRCh38
NC_000019.9:g.7735475G>C , CM000681.1:g.7735475G>C
GRCh37
NC_000019.8:g.7641475G>C
NCBI36
NG_023447.1:g.6504G>C
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