Canonical Allele Identifier: CA2766757881
Gene: CWC27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.65051837A>T , CM000667.2:g.65051837A>T GRCh38
NC_000005.9:g.64347664A>T , CM000667.1:g.64347664A>T GRCh37
NC_000005.8:g.64383420A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000693303.1:c.1153-47415A>T ENSP00000508557.1:n.1153-47415A>T