Canonical Allele Identifier: CA120344848

Gene: CWC27

Linked Data

• dbSNP Id: rs1036620661
• MyVariant Identifiers: chr5:g.64347647T>C (hg19) ; chr5:g.65051820T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.65051820T>C , CM000667.2:g.65051820T>C	GRCh38
NC_000005.9:g.64347647T>C , CM000667.1:g.64347647T>C	GRCh37
NC_000005.8:g.64383403T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000693303.1:c.1153-47432T>C	ENSP00000508557.1:n.1153-47432T>C