ClinGen Allele Registry
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Canonical Allele Identifier:
CA137031841
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.32690302T>C
GRCh37
chr6:g.32658079T>C
Linked Data - Sequence & Population
gnomAD v2:
6:32658079 T / C
gnomAD v3:
6:32690302 T / C
gnomAD v4:
chr6-32690302-T-C
Joint Max Group AF
0.25724904 (SAS)
Genomes Max Group AF
0.25724904 (SAS)
Linked Data - NCBI & NCI
dbSNP:
7775228
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.32690302T>C , CM000668.2:g.32690302T>C
GRCh38
NC_000006.11:g.32658079T>C , CM000668.1:g.32658079T>C
GRCh37
NC_000006.10:g.32766057T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'