Canonical Allele Identifier: CA2428353426
Gene: WAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48681784T= , CM000685.2:g.48681784T= GRCh38
NC_000023.10:g.48540173T= , CM000685.1:g.48540173T= GRCh37
NC_000023.9:g.48425117T= NCBI36
NG_007877.1:g.2988T= , LRG_125:g.2988T=

Transcript Alleles

HGVS Amino-acid change
ENST00000698625.1:c.-34-2036T= ENSP00000513844.1:n.-34-2036T=
ENST00000450772.5:c.-130-1484T= ENSP00000410537.1:n.-130-1484T=