Canonical Allele Identifier: CA641510470
Gene: WAS HGNC NCBI

Linked Data

dbSNP Id: rs1424439981
gnomAD v2: X-48542153-A-G
gnomAD v3: X-48683764-A-G
gnomAD v4: X-48683764-A-G
MyVariant Identifiers: chrX:g.48542153A>G (hg19) chrX:g.48683764A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48683764A>G , CM000685.2:g.48683764A>G GRCh38
NC_000023.10:g.48542153A>G , CM000685.1:g.48542153A>G GRCh37
NC_000023.9:g.48427097A>G NCBI36
NG_007877.1:g.4968A>G , LRG_125:g.4968A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698625.1:c.-34-56A>G ENSP00000513844.1:n.-34-56A>G
ENST00000450772.5:c.-34-56A>G ENSP00000410537.1:n.-34-56A>G
XM_017029786.1:c.-90A>G XP_016885275.1:n.-90A>G
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