Canonical Allele Identifier: CA2428354111
Gene: WAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48683718G= , CM000685.2:g.48683718G= GRCh38
NC_000023.10:g.48542107G= , CM000685.1:g.48542107G= GRCh37
NC_000023.9:g.48427051G= NCBI36
NG_007877.1:g.4922G= , LRG_125:g.4922G=

Transcript Alleles

HGVS Amino-acid change
ENST00000698625.1:c.-34-102G= ENSP00000513844.1:n.-34-102G=
ENST00000450772.5:c.-34-102G= ENSP00000410537.1:n.-34-102G=