ClinGen Allele Registry
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Canonical Allele Identifier:
CA306773916
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.29573489A>G
GRCh37
chr19:g.30064396A>G
Linked Data - Sequence & Population
gnomAD v2:
19:30064396 A / G
gnomAD v3:
19:29573489 A / G
gnomAD v4:
chr19-29573489-A-G
Joint Max Group AF
0.97593911 (EAS)
Genomes Max Group AF
0.97593911 (EAS)
Linked Data - NCBI & NCI
dbSNP:
7250581
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.29573489A>G , CM000681.2:g.29573489A>G
GRCh38
NC_000019.9:g.30064396A>G , CM000681.1:g.30064396A>G
GRCh37
NC_000019.8:g.34756236A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'