ClinGen Allele Registry
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Canonical Allele Identifier:
CA330732280
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrX:g.67350335T>C
GRCh37
chrX:g.66570177T>C
Linked Data - NCBI & NCI
dbSNP:
993245752
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.67350335T>C , CM000685.2:g.67350335T>C
GRCh38
NC_000023.10:g.66570177T>C , CM000685.1:g.66570177T>C
GRCh37
NC_000023.9:g.66486902T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'