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Canonical Allele Identifier:
CA331712178
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chrX:g.79393696C>T
GRCh37
chrX:g.78649193C>T
Linked Data - Sequence & Population
gnomAD v2:
X:78649193 C / T
gnomAD v3:
X:79393696 C / T
gnomAD v4:
chrX-79393696-C-T
Joint Max Group AF
0.57395402 (NFE)
Genomes Max Group AF
0.57395402 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1474563
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.79393696C>T , CM000685.2:g.79393696C>T
GRCh38
NC_000023.10:g.78649193C>T , CM000685.1:g.78649193C>T
GRCh37
NC_000023.9:g.78535849C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'