Canonical Allele Identifier: CA1551894139
Gene: CWC27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.65051772T= , CM000667.2:g.65051772T= GRCh38
NC_000005.9:g.64347599T= , CM000667.1:g.64347599T= GRCh37
NC_000005.8:g.64383355T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000693303.1:c.1153-47480T= ENSP00000508557.1:n.1153-47480T=