ClinGen Allele Registry
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Canonical Allele Identifier:
CA331603868
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrX:g.78328090G>T
GRCh37
chrX:g.77583587G>T
Linked Data - Sequence & Population
gnomAD v2:
X:77583587 G / T
gnomAD v3:
X:78328090 G / T
gnomAD v4:
chrX-78328090-G-T
Joint Max Group AF
0.90352666 (AFR)
Genomes Max Group AF
0.90352666 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2637204
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.78328090G>T , CM000685.2:g.78328090G>T
GRCh38
NC_000023.10:g.77583587G>T , CM000685.1:g.77583587G>T
GRCh37
NC_000023.9:g.77470243G>T
NCBI36
NG_012809.1:g.4501C>A
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