ClinGen Allele Registry
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Canonical Allele Identifier:
CA12275952
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.99224138T>C
GRCh37
chr6:g.99672014T>C
Linked Data - Sequence & Population
gnomAD v2:
6:99672014 T / C
gnomAD v3:
6:99224138 T / C
gnomAD v4:
chr6-99224138-T-C
Joint Max Group AF
0.4848881 (EAS)
Genomes Max Group AF
0.4848881 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2132683
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.99224138T>C , CM000668.2:g.99224138T>C
GRCh38
NC_000006.11:g.99672014T>C , CM000668.1:g.99672014T>C
GRCh37
NC_000006.10:g.99778735T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'