Canonical Allele Identifier: CA2693642792
Gene: WAS HGNC NCBI

Linked Data

gnomAD v4: X-48683727-G-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48683727G>C , CM000685.2:g.48683727G>C GRCh38
NC_000023.10:g.48542116G>C , CM000685.1:g.48542116G>C GRCh37
NC_000023.9:g.48427060G>C NCBI36
NG_007877.1:g.4931G>C , LRG_125:g.4931G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000698625.1:c.-34-93G>C ENSP00000513844.1:n.-34-93G>C
ENST00000450772.5:c.-34-93G>C ENSP00000410537.1:n.-34-93G>C
Search 100 bp 5'
Search 100 bp 3'