Canonical Allele Identifier: CA1551894178
Gene: CWC27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.65051867G= , CM000667.2:g.65051867G= GRCh38
NC_000005.9:g.64347694G= , CM000667.1:g.64347694G= GRCh37
NC_000005.8:g.64383450G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000693303.1:c.1153-47385G= ENSP00000508557.1:n.1153-47385G=