ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA12243616
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.94446700C>T
GRCh37
chr6:g.95156418C>T
Linked Data - Sequence & Population
gnomAD v2:
6:95156418 C / T
gnomAD v3:
6:94446700 C / T
gnomAD v4:
chr6-94446700-C-T
Joint Max Group AF
0.23268458 (NFE)
Genomes Max Group AF
0.23269517 (NFE)
Exomes Max Group AF
0.05110505 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2224003
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.94446700C>T , CM000668.2:g.94446700C>T
GRCh38
NC_000006.11:g.95156418C>T , CM000668.1:g.95156418C>T
GRCh37
NC_000006.10:g.95213139C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'