Canonical Allele Identifier: CA329099144
Gene: WAS HGNC NCBI

Linked Data

dbSNP Id: rs997493622
gnomAD v3: X-48681885-G-T
gnomAD v4: X-48681885-G-T
MyVariant Identifiers: chrX:g.48681885G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48681885G>T , CM000685.2:g.48681885G>T GRCh38
NC_000023.10:g.48540274G>T , CM000685.1:g.48540274G>T GRCh37
NC_000023.9:g.48425218G>T NCBI36
NG_007877.1:g.3089G>T , LRG_125:g.3089G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698625.1:c.-34-1935G>T ENSP00000513844.1:n.-34-1935G>T
ENST00000450772.5:c.-130-1383G>T ENSP00000410537.1:n.-130-1383G>T
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