Canonical Allele Identifier: CA1551894117
Gene: CWC27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.65051699C= , CM000667.2:g.65051699C= GRCh38
NC_000005.9:g.64347526C= , CM000667.1:g.64347526C= GRCh37
NC_000005.8:g.64383282C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000693303.1:c.1153-47553C= ENSP00000508557.1:n.1153-47553C=