ClinGen Allele Registry
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Canonical Allele Identifier:
CA16376246
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr9:g.134919852C>T
GRCh37
chr9:g.137811698C>T
Linked Data - Sequence & Population
gnomAD v2:
9:137811698 C / T
gnomAD v3:
9:134919852 C / T
gnomAD v4:
chr9-134919852-C-T
Joint Max Group AF
0.6203684 (NFE)
Genomes Max Group AF
0.6203684 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2989727
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.134919852C>T , CM000671.2:g.134919852C>T
GRCh38
NC_000009.11:g.137811698C>T , CM000671.1:g.137811698C>T
GRCh37
NC_000009.10:g.136951519C>T
NCBI36
NG_046982.2:g.3109G>A
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