Canonical Allele Identifier: CA1076893344
Gene: CWC27 HGNC NCBI

Linked Data

dbSNP Id: rs947736083
gnomAD v3: 5-65051765-C-T
gnomAD v4: 5-65051765-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.65051765C>T , CM000667.2:g.65051765C>T GRCh38
NC_000005.9:g.64347592C>T , CM000667.1:g.64347592C>T GRCh37
NC_000005.8:g.64383348C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000693303.1:c.1153-47487C>T ENSP00000508557.1:n.1153-47487C>T
Search 100 bp 5'
Search 100 bp 3'