ClinGen Allele Registry
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Canonical Allele Identifier:
CA136392776
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.22285845G>A
GRCh37
chr6:g.22286074G>A
Linked Data - Sequence & Population
gnomAD v2:
6:22286074 G / A
gnomAD v3:
6:22285845 G / A
gnomAD v4:
chr6-22285845-G-A
Joint Max Group AF
0.22229898 (EAS)
Genomes Max Group AF
0.22229898 (EAS)
Linked Data - NCBI & NCI
dbSNP:
10946545
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.22285845G>A , CM000668.2:g.22285845G>A
GRCh38
NC_000006.11:g.22286074G>A , CM000668.1:g.22286074G>A
GRCh37
NC_000006.10:g.22394053G>A
NCBI36
NG_029819.1:g.22009C>T
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