ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA85405972
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr3:g.144621363C>T
GRCh37
chr3:g.144340205C>T
Linked Data - Sequence & Population
gnomAD v2:
3:144340205 C / T
gnomAD v3:
3:144621363 C / T
gnomAD v4:
chr3-144621363-C-T
Joint Max Group AF
0.43755601 (NFE)
Genomes Max Group AF
0.43755601 (NFE)
Linked Data - NCBI & NCI
dbSNP:
800082
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.144621363C>T , CM000665.2:g.144621363C>T
GRCh38
NC_000003.11:g.144340205C>T , CM000665.1:g.144340205C>T
GRCh37
NC_000003.10:g.145822895C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'