ClinGen Allele Registry
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Canonical Allele Identifier:
CA12186357
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.29938914A>G
GRCh37
chr6:g.29906691A>G
Linked Data - Sequence & Population
gnomAD v2:
6:29906691 A / G
gnomAD v3:
6:29938914 A / G
gnomAD v4:
chr6-29938914-A-G
Joint Max Group AF
0.65450884 (EAS)
Genomes Max Group AF
0.65450884 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2860580
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.29938914A>G , CM000668.2:g.29938914A>G
GRCh38
NC_000006.11:g.29906691A>G , CM000668.1:g.29906691A>G
GRCh37
NC_000006.10:g.30014670A>G
NCBI36
NG_029217.2:g.1445A>G
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