ClinGen Allele Registry
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Canonical Allele Identifier:
CA870274803
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrX:g.114583441G>A
Linked Data - Sequence & Population
gnomAD v3:
X:114583441 G / A
gnomAD v4:
chrX-114583441-G-A
Linked Data - NCBI & NCI
dbSNP:
521018
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.114583441G>A , CM000685.2:g.114583441G>A
GRCh38
NG_012082.2:g.4357G>A
NG_012082.3:g.4357G>A
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