Canonical Allele Identifier: CA2428353419
Gene: WAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48681772C= , CM000685.2:g.48681772C= GRCh38
NC_000023.10:g.48540161C= , CM000685.1:g.48540161C= GRCh37
NC_000023.9:g.48425105C= NCBI36
NG_007877.1:g.2976C= , LRG_125:g.2976C=

Transcript Alleles

HGVS Amino-acid change
ENST00000698625.1:c.-34-2048C= ENSP00000513844.1:n.-34-2048C=
ENST00000450772.5:c.-130-1496C= ENSP00000410537.1:n.-130-1496C=