ClinGen Allele Registry
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Canonical Allele Identifier:
CA337276700
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrX:g.154010439C>A
GRCh37
chrX:g.153275890C>A
Linked Data - Sequence & Population
gnomAD v2:
X:153275890 C / A
gnomAD v3:
X:154010439 C / A
gnomAD v4:
chrX-154010439-C-A
Joint Max Group AF
0.79946774 (NFE)
Genomes Max Group AF
0.79846618 (NFE)
Exomes Max Group AF
0.79315494 (NFE)
Linked Data - NCBI & NCI
dbSNP:
3027898
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.154010439C>A , CM000685.2:g.154010439C>A
GRCh38
NC_000023.10:g.153275890C>A , CM000685.1:g.153275890C>A
GRCh37
NC_000023.9:g.152929084C>A
NCBI36
NG_008387.1:g.14453G>T
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