Canonical Allele Identifier: CA2428354130
Gene: WAS HGNC NCBI

Linked Data

dbSNP Id: rs1372471501

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48683790C>G , CM000685.2:g.48683790C>G GRCh38
NC_000023.10:g.48542179C>G , CM000685.1:g.48542179C>G GRCh37
NC_000023.9:g.48427123C>G NCBI36
NG_007877.1:g.4994C>G , LRG_125:g.4994C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000698625.1:c.-34-30C>G ENSP00000513844.1:n.-34-30C>G
ENST00000376701.4:c.-64C>G ENSP00000365891.4:n.-64C>G
ENST00000450772.5:c.-34-30C>G ENSP00000410537.1:n.-34-30C>G
XM_011543977.1:c.-64C>G XP_011542279.1:n.-64C>G
XM_017029786.1:c.-64C>G XP_016885275.1:n.-64C>G