Canonical Allele Identifier: CA918690117
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1588978632
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62528653_62528654insT , CM000672.2:g.62528653_62528654insT GRCh38
NC_000010.10:g.64288412_64288413insT , CM000672.1:g.64288412_64288413insT GRCh37
NC_000010.9:g.63958418_63958419insT NCBI36
NG_021209.1:g.159497_159498insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.981+68856_981+68857insT ENSP00000502188.1:n.981+68856_981+68857insT
ENST00000395251.5:c.-185+8056_-185+8057insT ENSP00000378672.1:n.-185+8056_-185+8057insT
ENST00000410046.7:c.981+68856_981+68857insT ENSP00000387091.3:n.981+68856_981+68857insT
NM_199451.2:c.981+68856_981+68857insT NP_955523.1:n.981+68856_981+68857insT
NM_199452.3:c.-185+8056_-185+8057insT NP_955524.3:n.-185+8056_-185+8057insT
XM_017015937.2:c.982-15556_982-15555insT XP_016871426.1:n.982-15556_982-15555insT
NM_199451.3:c.981+68856_981+68857insT NP_955523.1:n.981+68856_981+68857insT
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