Canonical Allele Identifier: CA2594481287
Gene: WAS HGNC NCBI

Linked Data

gnomAD v3: X-48683701-G-T
gnomAD v4: X-48683701-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48683701G>T , CM000685.2:g.48683701G>T GRCh38
NC_000023.10:g.48542090G>T , CM000685.1:g.48542090G>T GRCh37
NC_000023.9:g.48427034G>T NCBI36
NG_007877.1:g.4905G>T , LRG_125:g.4905G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000698625.1:c.-34-119G>T ENSP00000513844.1:n.-34-119G>T
ENST00000450772.5:c.-34-119G>T ENSP00000410537.1:n.-34-119G>T
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