Canonical Allele Identifier: CA2428353422
Gene: WAS HGNC NCBI

Linked Data

dbSNP Id: rs2062400906

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48681778G>C , CM000685.2:g.48681778G>C GRCh38
NC_000023.10:g.48540167G>C , CM000685.1:g.48540167G>C GRCh37
NC_000023.9:g.48425111G>C NCBI36
NG_007877.1:g.2982G>C , LRG_125:g.2982G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698625.1:c.-34-2042G>C ENSP00000513844.1:n.-34-2042G>C
ENST00000450772.5:c.-130-1490G>C ENSP00000410537.1:n.-130-1490G>C