Canonical Allele Identifier: CA329099126
Gene: WAS HGNC NCBI

Linked Data

dbSNP Id: rs1041106522
MyVariant Identifiers: chrX:g.48681822C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48681822C>T , CM000685.2:g.48681822C>T GRCh38
NC_000023.10:g.48540211C>T , CM000685.1:g.48540211C>T GRCh37
NC_000023.9:g.48425155C>T NCBI36
NG_007877.1:g.3026C>T , LRG_125:g.3026C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698625.1:c.-34-1998C>T ENSP00000513844.1:n.-34-1998C>T
ENST00000450772.5:c.-130-1446C>T ENSP00000410537.1:n.-130-1446C>T
Search 100 bp 5'
Search 100 bp 3'