ClinGen Allele Registry
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Canonical Allele Identifier:
CA336583557
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chrX:g.142272785C>T
GRCh37
chrX:g.141360571C>T
Linked Data - Sequence & Population
gnomAD v2:
X:141360571 C / T
gnomAD v3:
X:142272785 C / T
gnomAD v4:
X:142272785 C / T
Linked Data - NCBI & NCI
dbSNP:
5954596
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.142272785C>T , CM000685.2:g.142272785C>T
GRCh38
NC_000023.10:g.141360571C>T , CM000685.1:g.141360571C>T
GRCh37
NC_000023.9:g.141188237C>T
NCBI36
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