Canonical Allele Identifier: CA1551894151
Gene: CWC27 HGNC NCBI

Linked Data

dbSNP Id: rs1750515104
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.65051796A>G , CM000667.2:g.65051796A>G GRCh38
NC_000005.9:g.64347623A>G , CM000667.1:g.64347623A>G GRCh37
NC_000005.8:g.64383379A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000693303.1:c.1153-47456A>G ENSP00000508557.1:n.1153-47456A>G
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