ClinGen Allele Registry
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Canonical Allele Identifier:
CA15038575
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrX:g.151221459C>A
GRCh37
chrX:g.150389931C>A
Linked Data - Sequence & Population
gnomAD v2:
X:150389931 C / A
gnomAD v3:
X:151221459 C / A
gnomAD v4:
chrX-151221459-C-A
Joint Max Group AF
0.79291465 (AFR)
Genomes Max Group AF
0.79291465 (AFR)
Linked Data - NCBI & NCI
dbSNP:
1149374
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.151221459C>A , CM000685.2:g.151221459C>A
GRCh38
NC_000023.10:g.150389931C>A , CM000685.1:g.150389931C>A
GRCh37
NC_000023.9:g.150140589C>A
NCBI36
Search 100 bp 5'
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