Canonical Allele Identifier: CA641510466
Gene: WAS HGNC NCBI

Linked Data

dbSNP Id: rs1557006176
gnomAD v2: X-48542095-C-T
gnomAD v3: X-48683706-C-T
gnomAD v4: X-48683706-C-T
MyVariant Identifiers: chrX:g.48542095C>T (hg19) chrX:g.48683706C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48683706C>T , CM000685.2:g.48683706C>T GRCh38
NC_000023.10:g.48542095C>T , CM000685.1:g.48542095C>T GRCh37
NC_000023.9:g.48427039C>T NCBI36
NG_007877.1:g.4910C>T , LRG_125:g.4910C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000698625.1:c.-34-114C>T ENSP00000513844.1:n.-34-114C>T
ENST00000450772.5:c.-34-114C>T ENSP00000410537.1:n.-34-114C>T
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