Canonical Allele Identifier: CA2840872400
Gene: WAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48683796T>C , CM000685.2:g.48683796T>C GRCh38
NC_000023.10:g.48542185T>C , CM000685.1:g.48542185T>C GRCh37
NC_000023.9:g.48427129T>C NCBI36
NG_007877.1:g.5000T>C , LRG_125:g.5000T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698625.1:c.-34-24T>C ENSP00000513844.1:n.-34-24T>C
ENST00000376701.4:c.-58T>C ENSP00000365891.4:n.-58T>C
ENST00000450772.5:c.-34-24T>C ENSP00000410537.1:n.-34-24T>C
XM_011543977.1:c.-58T>C XP_011542279.1:n.-58T>C
XM_011543977.2:c.-58T>C XP_011542279.1:n.-58T>C
XM_017029786.1:c.-58T>C XP_016885275.1:n.-58T>C