Canonical Allele Identifier: CA2428353425
Gene: WAS HGNC NCBI

Linked Data

dbSNP Id: rs2062400928
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48681783T>C , CM000685.2:g.48681783T>C GRCh38
NC_000023.10:g.48540172T>C , CM000685.1:g.48540172T>C GRCh37
NC_000023.9:g.48425116T>C NCBI36
NG_007877.1:g.2987T>C , LRG_125:g.2987T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000698625.1:c.-34-2037T>C ENSP00000513844.1:n.-34-2037T>C
ENST00000450772.5:c.-130-1485T>C ENSP00000410537.1:n.-130-1485T>C
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