ClinGen Allele Registry
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Canonical Allele Identifier:
CA12959380
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr9:g.79274443G>C
GRCh37
chr9:g.81889358G>C
Linked Data - Sequence & Population
gnomAD v2:
9:81889358 G / C
gnomAD v3:
9:79274443 G / C
gnomAD v4:
chr9-79274443-G-C
Joint Max Group AF
0.61072486 (SAS)
Genomes Max Group AF
0.61072486 (SAS)
Linked Data - NCBI & NCI
dbSNP:
2769967
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.79274443G>C , CM000671.2:g.79274443G>C
GRCh38
NC_000009.11:g.81889358G>C , CM000671.1:g.81889358G>C
GRCh37
NC_000009.10:g.81079178G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'