Canonical Allele Identifier: CA999467094
Gene: CDC42 HGNC NCBI
CDC42-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1022111619
gnomAD v3: 1-22035275-C-G
gnomAD v4: 1-22035275-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.22035275C>G , CM000663.2:g.22035275C>G GRCh38
NC_000001.10:g.22361768C>G , CM000663.1:g.22361768C>G GRCh37
NC_000001.9:g.22234355C>G NCBI36
NG_047042.3:g.14765C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000695855.1:c.-51+9903C>G ENSP00000512220.1:n.-51+9903C>G
ENST00000695856.1:c.-51+9636C>G ENSP00000512221.1:n.-51+9636C>G
ENST00000648594.1:c.-51+9636C>G (CDC42) ENSP00000497733.1:n.-51+9636C>G
XR_947048.1:n.84-3408G>C
XR_002958282.1:n.141-3408G>C (CDC42-AS1)
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