Canonical Allele Identifier: CA875913391
Gene: WAS HGNC NCBI

Linked Data

dbSNP Id: rs1318041275
gnomAD v3: X-48683694-T-C
gnomAD v4: X-48683694-T-C
MyVariant Identifiers: chrX:g.48683694T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48683694T>C , CM000685.2:g.48683694T>C GRCh38
NC_000023.10:g.48542083T>C , CM000685.1:g.48542083T>C GRCh37
NC_000023.9:g.48427027T>C NCBI36
NG_007877.1:g.4898T>C , LRG_125:g.4898T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000698625.1:c.-34-126T>C ENSP00000513844.1:n.-34-126T>C
ENST00000450772.5:c.-34-126T>C ENSP00000410537.1:n.-34-126T>C
Search 100 bp 5'
Search 100 bp 3'