Canonical Allele Identifier: CA120344840

Gene: CWC27

Linked Data

• dbSNP Id: rs764434627
• gnomAD v3: 5-65051717-G-A
• gnomAD v4: 5-65051717-G-A
• MyVariant Identifiers: chr5:g.64347544G>A (hg19) ; chr5:g.65051717G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.65051717G>A , CM000667.2:g.65051717G>A	GRCh38
NC_000005.9:g.64347544G>A , CM000667.1:g.64347544G>A	GRCh37
NC_000005.8:g.64383300G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000693303.1:c.1153-47535G>A	ENSP00000508557.1:n.1153-47535G>A