Canonical Allele Identifier: CA560122499

Gene: CWC27

Linked Data

• dbSNP Id: rs2194218
• gnomAD v2: 5-64347662-G-A
• gnomAD v3: 5-65051835-G-A
• gnomAD v4: 5-65051835-G-A
• MyVariant Identifiers: chr5:g.64347662G>A (hg19) ; chr5:g.65051835G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.65051835G>A , CM000667.2:g.65051835G>A	GRCh38
NC_000005.9:g.64347662G>A , CM000667.1:g.64347662G>A	GRCh37
NC_000005.8:g.64383418G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000693303.1:c.1153-47417G>A	ENSP00000508557.1:n.1153-47417G>A