Canonical Allele Identifier: CA1551894130
Gene: CWC27 HGNC NCBI

Linked Data

dbSNP Id: rs1750514357
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.65051743C>A , CM000667.2:g.65051743C>A GRCh38
NC_000005.9:g.64347570C>A , CM000667.1:g.64347570C>A GRCh37
NC_000005.8:g.64383326C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000693303.1:c.1153-47509C>A ENSP00000508557.1:n.1153-47509C>A
Search 100 bp 5'
Search 100 bp 3'