ClinGen Allele Registry
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Canonical Allele Identifier:
CA199249807
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr9:g.118580943A>C
GRCh37
chr9:g.121343221A>C
Linked Data - Sequence & Population
gnomAD v2:
9:121343221 A / C
gnomAD v3:
9:118580943 A / C
gnomAD v4:
chr9-118580943-A-C
Joint Max Group AF
0.25296686 (SAS)
Genomes Max Group AF
0.25296686 (SAS)
Linked Data - NCBI & NCI
dbSNP:
10125157
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.118580943A>C , CM000671.2:g.118580943A>C
GRCh38
NC_000009.11:g.121343221A>C , CM000671.1:g.121343221A>C
GRCh37
NC_000009.10:g.120383042A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'