ClinGen Allele Registry
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Canonical Allele Identifier:
CA198223966
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.105678261T>C
GRCh37
chr9:g.108440542T>C
Linked Data - Sequence & Population
gnomAD v2:
9:108440542 T / C
gnomAD v3:
9:105678261 T / C
gnomAD v4:
chr9-105678261-T-C
Joint Max Group AF
0.17539908 (AFR)
Genomes Max Group AF
0.17539908 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10120372
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.105678261T>C , CM000671.2:g.105678261T>C
GRCh38
NC_000009.11:g.108440542T>C , CM000671.1:g.108440542T>C
GRCh37
NC_000009.10:g.107480363T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'