Canonical Allele Identifier: CA2693642805
Gene: WAS HGNC NCBI

Linked Data

gnomAD v4: X-48683753-T-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48683753T>A , CM000685.2:g.48683753T>A GRCh38
NC_000023.10:g.48542142T>A , CM000685.1:g.48542142T>A GRCh37
NC_000023.9:g.48427086T>A NCBI36
NG_007877.1:g.4957T>A , LRG_125:g.4957T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000698625.1:c.-34-67T>A ENSP00000513844.1:n.-34-67T>A
ENST00000450772.5:c.-34-67T>A ENSP00000410537.1:n.-34-67T>A
XM_017029786.1:c.-101T>A XP_016885275.1:n.-101T>A
Search 100 bp 5'
Search 100 bp 3'