ClinGen Allele Registry
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Canonical Allele Identifier:
CA308127729
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.38645848G>A
GRCh37
chr19:g.39136488G>A
Linked Data - Sequence & Population
gnomAD v2:
19:39136488 G / A
gnomAD v3:
19:38645848 G / A
gnomAD v4:
chr19-38645848-G-A
Joint Max Group AF
0.00119311 (EAS)
Genomes Max Group AF
0.00119311 (EAS)
Linked Data - NCBI & NCI
dbSNP:
569306979
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.38645848G>A , CM000681.2:g.38645848G>A
GRCh38
NC_000019.9:g.39136488G>A , CM000681.1:g.39136488G>A
GRCh37
NC_000019.8:g.43828328G>A
NCBI36
NG_007082.2:g.3162G>A
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