Canonical Allele Identifier: CA1551894157
Gene: CWC27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.65051825A= , CM000667.2:g.65051825A= GRCh38
NC_000005.9:g.64347652A= , CM000667.1:g.64347652A= GRCh37
NC_000005.8:g.64383408A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000693303.1:c.1153-47427A= ENSP00000508557.1:n.1153-47427A=