Canonical Allele Identifier: CA1551894174
Gene: CWC27 HGNC NCBI

Linked Data

dbSNP Id: rs1750516016

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.65051844C>T , CM000667.2:g.65051844C>T GRCh38
NC_000005.9:g.64347671C>T , CM000667.1:g.64347671C>T GRCh37
NC_000005.8:g.64383427C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000693303.1:c.1153-47408C>T ENSP00000508557.1:n.1153-47408C>T