Canonical Allele Identifier: CA2547135660
Gene: CWC27 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.65051739A>T , CM000667.2:g.65051739A>T GRCh38
NC_000005.9:g.64347566A>T , CM000667.1:g.64347566A>T GRCh37
NC_000005.8:g.64383322A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000693303.1:c.1153-47513A>T ENSP00000508557.1:n.1153-47513A>T
Search 100 bp 5'
Search 100 bp 3'