Canonical Allele Identifier: CA1551894120
Gene: CWC27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.65051708A= , CM000667.2:g.65051708A= GRCh38
NC_000005.9:g.64347535A= , CM000667.1:g.64347535A= GRCh37
NC_000005.8:g.64383291A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000693303.1:c.1153-47544A= ENSP00000508557.1:n.1153-47544A=