ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA11668813
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.174465154C>A
GRCh37
chr4:g.175386305C>A
Linked Data - Sequence & Population
gnomAD v2:
4:175386305 C / A
gnomAD v3:
4:174465154 C / A
gnomAD v4:
chr4-174465154-C-A
Joint Max Group AF
0.33961848 (NFE)
Genomes Max Group AF
0.33961848 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2332897
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.174465154C>A , CM000666.2:g.174465154C>A
GRCh38
NC_000004.11:g.175386305C>A , CM000666.1:g.175386305C>A
GRCh37
NC_000004.10:g.175622880C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'