ClinGen Allele Registry
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Canonical Allele Identifier:
CA642371590
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrX:g.67350246G>T
GRCh37
chrX:g.66570088G>T
Linked Data - Sequence & Population
gnomAD v2:
X:66570088 G / T
gnomAD v3:
X:67350246 G / T
gnomAD v4:
chrX-67350246-G-T
Linked Data - NCBI & NCI
dbSNP:
1334336211
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.67350246G>T , CM000685.2:g.67350246G>T
GRCh38
NC_000023.10:g.66570088G>T , CM000685.1:g.66570088G>T
GRCh37
NC_000023.9:g.66486813G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'