Canonical Allele Identifier: CA2693642779
Gene: WAS HGNC NCBI

Linked Data

gnomAD v4: X-48683711-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48683711C>A , CM000685.2:g.48683711C>A GRCh38
NC_000023.10:g.48542100C>A , CM000685.1:g.48542100C>A GRCh37
NC_000023.9:g.48427044C>A NCBI36
NG_007877.1:g.4915C>A , LRG_125:g.4915C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000698625.1:c.-34-109C>A ENSP00000513844.1:n.-34-109C>A
ENST00000450772.5:c.-34-109C>A ENSP00000410537.1:n.-34-109C>A
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