ClinGen Allele Registry
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Canonical Allele Identifier:
CA335926120
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrX:g.133003128T>C
GRCh37
chrX:g.132137156T>C
Linked Data - Sequence & Population
gnomAD v2:
X:132137156 T / C
gnomAD v3:
X:133003128 T / C
gnomAD v4:
chrX-133003128-T-C
Joint Max Group AF
0.07944181 (EAS)
Genomes Max Group AF
0.07944181 (EAS)
Linked Data - NCBI & NCI
dbSNP:
17324272
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.133003128T>C , CM000685.2:g.133003128T>C
GRCh38
NC_000023.10:g.132137156T>C , CM000685.1:g.132137156T>C
GRCh37
NC_000023.9:g.131964822T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'