ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA217909831
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr11:g.14900334G>A
GRCh37
chr11:g.14921880G>A
Linked Data - Sequence & Population
gnomAD v2:
11:14921880 G / A
gnomAD v3:
11:14900334 G / A
gnomAD v4:
chr11-14900334-G-A
Joint Max Group AF
0.46345357 (NFE)
Genomes Max Group AF
0.46345357 (NFE)
Linked Data - NCBI & NCI
dbSNP:
10766197
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.14900334G>A , CM000673.2:g.14900334G>A
GRCh38
NC_000011.9:g.14921880G>A , CM000673.1:g.14921880G>A
GRCh37
NC_000011.8:g.14878456G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'