Canonical Allele Identifier: CA2428353408
Gene: WAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48681726A= , CM000685.2:g.48681726A= GRCh38
NC_000023.10:g.48540115A= , CM000685.1:g.48540115A= GRCh37
NC_000023.9:g.48425059A= NCBI36
NG_007877.1:g.2930A= , LRG_125:g.2930A=

Transcript Alleles

HGVS Amino-acid change
ENST00000698625.1:c.-34-2094A= ENSP00000513844.1:n.-34-2094A=
ENST00000450772.5:c.-130-1542A= ENSP00000410537.1:n.-130-1542A=