Canonical Allele Identifier: CA1551894134
Gene: CWC27 HGNC NCBI

Linked Data

dbSNP Id: rs1750514527

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.65051755T>G , CM000667.2:g.65051755T>G GRCh38
NC_000005.9:g.64347582T>G , CM000667.1:g.64347582T>G GRCh37
NC_000005.8:g.64383338T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000693303.1:c.1153-47497T>G ENSP00000508557.1:n.1153-47497T>G