Canonical Allele Identifier: CA2428353411
Gene: WAS HGNC NCBI

Linked Data

dbSNP Id: rs2062400808
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48681738C>T , CM000685.2:g.48681738C>T GRCh38
NC_000023.10:g.48540127C>T , CM000685.1:g.48540127C>T GRCh37
NC_000023.9:g.48425071C>T NCBI36
NG_007877.1:g.2942C>T , LRG_125:g.2942C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000698625.1:c.-34-2082C>T ENSP00000513844.1:n.-34-2082C>T
ENST00000450772.5:c.-130-1530C>T ENSP00000410537.1:n.-130-1530C>T
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