Canonical Allele Identifier: CA2428354122
Gene: WAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48683760T= , CM000685.2:g.48683760T= GRCh38
NC_000023.10:g.48542149T= , CM000685.1:g.48542149T= GRCh37
NC_000023.9:g.48427093T= NCBI36
NG_007877.1:g.4964T= , LRG_125:g.4964T=

Transcript Alleles

HGVS Amino-acid change
ENST00000698625.1:c.-34-60T= ENSP00000513844.1:n.-34-60T=
ENST00000450772.5:c.-34-60T= ENSP00000410537.1:n.-34-60T=
XM_017029786.1:c.-94T= XP_016885275.1:n.-94T=