Canonical Allele Identifier: CA2428354127
Gene: WAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48683778T= , CM000685.2:g.48683778T= GRCh38
NC_000023.10:g.48542167T= , CM000685.1:g.48542167T= GRCh37
NC_000023.9:g.48427111T= NCBI36
NG_007877.1:g.4982T= , LRG_125:g.4982T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698625.1:c.-34-42T= ENSP00000513844.1:n.-34-42T=
ENST00000450772.5:c.-34-42T= ENSP00000410537.1:n.-34-42T=
XM_017029786.1:c.-76T= XP_016885275.1:n.-76T=