Canonical Allele Identifier: CA120344841

Gene: CWC27

Linked Data

• dbSNP Id: rs761241033
• gnomAD v3: 5-65051723-G-C
• gnomAD v4: 5-65051723-G-C
• MyVariant Identifiers: chr5:g.64347550G>C (hg19) ; chr5:g.65051723G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.65051723G>C , CM000667.2:g.65051723G>C	GRCh38
NC_000005.9:g.64347550G>C , CM000667.1:g.64347550G>C	GRCh37
NC_000005.8:g.64383306G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000693303.1:c.1153-47529G>C	ENSP00000508557.1:n.1153-47529G>C