ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA11478895
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr3:g.102055199G>C
GRCh37
chr3:g.101774043G>C
Linked Data - Sequence & Population
gnomAD v2:
3:101774043 G / C
gnomAD v3:
3:102055199 G / C
gnomAD v4:
chr3-102055199-G-C
Joint Max Group AF
0.59115638 (EAS)
Genomes Max Group AF
0.59115638 (EAS)
Linked Data - NCBI & NCI
dbSNP:
991258
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.102055199G>C , CM000665.2:g.102055199G>C
GRCh38
NC_000003.11:g.101774043G>C , CM000665.1:g.101774043G>C
GRCh37
NC_000003.10:g.103256733G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'