ClinGen Allele Registry
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Canonical Allele Identifier:
CA308192760
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.39252464G>A
GRCh37
chr19:g.39743104G>A
Linked Data - Sequence & Population
gnomAD v3:
19:39252464 G / A
gnomAD v4:
chr19-39252464-G-A
Joint Max Group AF
0.0000192 (AFR)
Genomes Max Group AF
0.0000192 (AFR)
Linked Data - NCBI & NCI
dbSNP:
962078528
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.39252464G>A , CM000681.2:g.39252464G>A
GRCh38
NC_000019.9:g.39743104G>A , CM000681.1:g.39743104G>A
GRCh37
NC_000019.8:g.44434944G>A
NCBI36
NG_055295.1:g.1393C>T
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