ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA15236139
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.128478439C>T
GRCh37
chr3:g.128197282C>T
Linked Data - Sequence & Population
gnomAD v2:
3:128197282 C / T
gnomAD v3:
3:128478439 C / T
gnomAD v4:
chr3-128478439-C-T
Joint Max Group AF
0.74950945 (AFR)
Genomes Max Group AF
0.74950945 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1573949
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.128478439C>T , CM000665.2:g.128478439C>T
GRCh38
NC_000003.11:g.128197282C>T , CM000665.1:g.128197282C>T
GRCh37
NC_000003.10:g.129679972C>T
NCBI36
NG_029334.1:g.19749G>A , LRG_295:g.19749G>A
Search 100 bp 5'
Search 100 bp 3'