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Canonical Allele Identifier:
CA333680785
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrX:g.98609356T>C
GRCh37
chrX:g.97864354T>C
Linked Data - Sequence & Population
gnomAD v2:
X:97864354 T / C
gnomAD v3:
X:98609356 T / C
gnomAD v4:
chrX-98609356-T-C
Joint Max Group AF
0.92795057 (AFR)
Genomes Max Group AF
0.92795057 (AFR)
Linked Data - NCBI & NCI
dbSNP:
4827947
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.98609356T>C , CM000685.2:g.98609356T>C
GRCh38
NC_000023.10:g.97864354T>C , CM000685.1:g.97864354T>C
GRCh37
NC_000023.9:g.97751010T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'