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Canonical Allele Identifier:
CA16010539
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrX:g.45874916G>C
GRCh37
chrX:g.45734351G>C
Linked Data - Sequence & Population
gnomAD v2:
X:45734351 G / C
gnomAD v3:
X:45874916 G / C
gnomAD v4:
chrX-45874916-G-C
Joint Max Group AF
0.87645451 (EAS)
Genomes Max Group AF
0.87645451 (EAS)
Linked Data - NCBI & NCI
dbSNP:
6521054
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.45874916G>C , CM000685.2:g.45874916G>C
GRCh38
NC_000023.10:g.45734351G>C , CM000685.1:g.45734351G>C
GRCh37
NC_000023.9:g.45619295G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'