Canonical Allele Identifier: CA667306027
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1229654552
MyVariant Identifiers: chr10:g.64369952G>T (hg19) chr10:g.62610193G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62610193G>T , CM000672.2:g.62610193G>T GRCh38
NC_000010.10:g.64369952G>T , CM000672.1:g.64369952G>T GRCh37
NC_000010.9:g.64039958G>T NCBI36
NG_021209.1:g.241037G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647733.1:c.982-12910G>T ENSP00000502188.1:n.982-12910G>T
ENST00000395251.5:c.-184-33549G>T ENSP00000378672.1:n.-184-33549G>T
ENST00000410046.7:c.982-12910G>T ENSP00000387091.3:n.982-12910G>T
NM_199451.2:c.982-12910G>T NP_955523.1:n.982-12910G>T
NM_199452.3:c.-184-33549G>T NP_955524.3:n.-184-33549G>T
NM_199451.3:c.982-12910G>T NP_955523.1:n.982-12910G>T
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