Canonical Allele Identifier: CA1551894176
Gene: CWC27 HGNC NCBI

Linked Data

dbSNP Id: rs1750516039

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.65051846G>A , CM000667.2:g.65051846G>A GRCh38
NC_000005.9:g.64347673G>A , CM000667.1:g.64347673G>A GRCh37
NC_000005.8:g.64383429G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000693303.1:c.1153-47406G>A ENSP00000508557.1:n.1153-47406G>A