Canonical Allele Identifier: CA329099802
Gene: WAS HGNC NCBI

Linked Data

dbSNP Id: rs782406499
gnomAD v2: X-48542103-C-A
gnomAD v3: X-48683714-C-A
gnomAD v4: X-48683714-C-A
MyVariant Identifiers: chrX:g.48542103C>A (hg19) chrX:g.48683714C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48683714C>A , CM000685.2:g.48683714C>A GRCh38
NC_000023.10:g.48542103C>A , CM000685.1:g.48542103C>A GRCh37
NC_000023.9:g.48427047C>A NCBI36
NG_007877.1:g.4918C>A , LRG_125:g.4918C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000698625.1:c.-34-106C>A ENSP00000513844.1:n.-34-106C>A
ENST00000450772.5:c.-34-106C>A ENSP00000410537.1:n.-34-106C>A
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