ClinGen Allele Registry
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Canonical Allele Identifier:
CA823766317
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.29974166C>G
GRCh37
chr6:g.29941943C>G
Linked Data - Sequence & Population
gnomAD v3:
6:29974166 C / G
gnomAD v4:
chr6-29974166-C-G
Joint Max Group AF
0.00011392 (AFR)
Genomes Max Group AF
0.00011392 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2523946
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.29974166C>G , CM000668.2:g.29974166C>G
GRCh38
NC_000006.11:g.29941943C>G , CM000668.1:g.29941943C>G
GRCh37
NC_000006.10:g.30049922C>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'