ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA12335613
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.132572626G>A
GRCh37
chr6:g.132893765G>A
Linked Data - Sequence & Population
gnomAD v2:
6:132893765 G / A
gnomAD v3:
6:132572626 G / A
gnomAD v4:
chr6-132572626-G-A
Joint Max Group AF
0.60634827 (SAS)
Genomes Max Group AF
0.60634827 (SAS)
Linked Data - NCBI & NCI
dbSNP:
4305746
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.132572626G>A , CM000668.2:g.132572626G>A
GRCh38
NC_000006.11:g.132893765G>A , CM000668.1:g.132893765G>A
GRCh37
NC_000006.10:g.132935458G>A
NCBI36
NG_016544.1:g.7305G>A
Search 100 bp 5'
Search 100 bp 3'