Canonical Allele Identifier: CA2572754387
Gene: CWC27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.65051801G>T , CM000667.2:g.65051801G>T GRCh38
NC_000005.9:g.64347628G>T , CM000667.1:g.64347628G>T GRCh37
NC_000005.8:g.64383384G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000693303.1:c.1153-47451G>T ENSP00000508557.1:n.1153-47451G>T