Canonical Allele Identifier: CA2428353424
Gene: WAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48681783T= , CM000685.2:g.48681783T= GRCh38
NC_000023.10:g.48540172T= , CM000685.1:g.48540172T= GRCh37
NC_000023.9:g.48425116T= NCBI36
NG_007877.1:g.2987T= , LRG_125:g.2987T=

Transcript Alleles

HGVS Amino-acid change
ENST00000698625.1:c.-34-2037T= ENSP00000513844.1:n.-34-2037T=
ENST00000450772.5:c.-130-1485T= ENSP00000410537.1:n.-130-1485T=