Canonical Allele Identifier: CA120344843

Gene: CWC27

Linked Data

• dbSNP Id: rs146117686
• gnomAD v2: 5-64347580-C-A
• gnomAD v3: 5-65051753-C-A
• gnomAD v4: 5-65051753-C-A
• MyVariant Identifiers: chr5:g.64347580C>A (hg19) ; chr5:g.65051753C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.65051753C>A , CM000667.2:g.65051753C>A	GRCh38
NC_000005.9:g.64347580C>A , CM000667.1:g.64347580C>A	GRCh37
NC_000005.8:g.64383336C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000693303.1:c.1153-47499C>A	ENSP00000508557.1:n.1153-47499C>A