Canonical Allele Identifier: CA2693642777

Gene: WAS

Linked Data

• gnomAD v4: X-48683709-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48683709G>T , CM000685.2:g.48683709G>T	GRCh38
NC_000023.10:g.48542098G>T , CM000685.1:g.48542098G>T	GRCh37
NC_000023.9:g.48427042G>T	NCBI36
NG_007877.1:g.4913G>T , LRG_125:g.4913G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000698625.1:c.-34-111G>T	ENSP00000513844.1:n.-34-111G>T
ENST00000450772.5:c.-34-111G>T	ENSP00000410537.1:n.-34-111G>T