Canonical Allele Identifier: CA813110969

Gene: CWC27

Linked Data

• dbSNP Id: rs1466232368
• MyVariant Identifiers: chr5:g.64347646C>T (hg19) ; chr5:g.65051819C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.65051819C>T , CM000667.2:g.65051819C>T	GRCh38
NC_000005.9:g.64347646C>T , CM000667.1:g.64347646C>T	GRCh37
NC_000005.8:g.64383402C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000693303.1:c.1153-47433C>T	ENSP00000508557.1:n.1153-47433C>T