Canonical Allele Identifier: CA2428353380
Gene: WAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48681640A= , CM000685.2:g.48681640A= GRCh38
NC_000023.10:g.48540029A= , CM000685.1:g.48540029A= GRCh37
NC_000023.9:g.48424973A= NCBI36
NG_007877.1:g.2844A= , LRG_125:g.2844A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698625.1:c.-34-2180A= ENSP00000513844.1:n.-34-2180A=
ENST00000450772.5:c.-130-1628A= ENSP00000410537.1:n.-130-1628A=