ClinGen Allele Registry
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Canonical Allele Identifier:
CA255284
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chrX:g.154182566A>C
GRCh37
chrX:g.153448055A>C
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000011256
ClinVar Variation:
10510
dbSNP:
724159983
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.154182566A>C , CM000685.2:g.154182566A>C
GRCh38
NC_000023.10:g.153448055A>C , CM000685.1:g.153448055A>C
GRCh37
NG_011606.1:g.4971A>C
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