Canonical Allele Identifier: CA2428353394
Gene: WAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48681688T= , CM000685.2:g.48681688T= GRCh38
NC_000023.10:g.48540077T= , CM000685.1:g.48540077T= GRCh37
NC_000023.9:g.48425021T= NCBI36
NG_007877.1:g.2892T= , LRG_125:g.2892T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698625.1:c.-34-2132T= ENSP00000513844.1:n.-34-2132T=
ENST00000450772.5:c.-130-1580T= ENSP00000410537.1:n.-130-1580T=