Canonical Allele Identifier: CA1245436042
Gene: CDC42EP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.37713399T= , CM000664.2:g.37713399T= GRCh38
NC_000002.11:g.37940542T= , CM000664.1:g.37940542T= GRCh37
NC_000002.10:g.37794046T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000453555.1:c.-333+6139A= ENSP00000398062.1:n.-333+6139A=