ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA11789317
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.126012137G>C
GRCh37
chr4:g.126933292G>C
Linked Data - Sequence & Population
gnomAD v2:
4:126933292 G / C
gnomAD v3:
4:126012137 G / C
gnomAD v4:
chr4-126012137-G-C
Joint Max Group AF
0.50354187 (AMR)
Genomes Max Group AF
0.50354187 (AMR)
Linked Data - NCBI & NCI
dbSNP:
1320267
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.126012137G>C , CM000666.2:g.126012137G>C
GRCh38
NC_000004.11:g.126933292G>C , CM000666.1:g.126933292G>C
GRCh37
NC_000004.10:g.127152742G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'