Canonical Allele Identifier: CA560122488
Gene: CWC27 HGNC NCBI

Linked Data

dbSNP Id: rs1228492248
gnomAD v2: 5-64347587-G-A
gnomAD v3: 5-65051760-G-A
gnomAD v4: 5-65051760-G-A
MyVariant Identifiers: chr5:g.64347587G>A (hg19) chr5:g.65051760G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.65051760G>A , CM000667.2:g.65051760G>A GRCh38
NC_000005.9:g.64347587G>A , CM000667.1:g.64347587G>A GRCh37
NC_000005.8:g.64383343G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000693303.1:c.1153-47492G>A ENSP00000508557.1:n.1153-47492G>A
Search 100 bp 5'
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