Canonical Allele Identifier: CA2428353456
Gene: WAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48681885G= , CM000685.2:g.48681885G= GRCh38
NC_000023.10:g.48540274G= , CM000685.1:g.48540274G= GRCh37
NC_000023.9:g.48425218G= NCBI36
NG_007877.1:g.3089G= , LRG_125:g.3089G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698625.1:c.-34-1935G= ENSP00000513844.1:n.-34-1935G=
ENST00000450772.5:c.-130-1383G= ENSP00000410537.1:n.-130-1383G=