Canonical Allele Identifier: CA1914620052
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1589019534

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62610349C>G , CM000672.2:g.62610349C>G GRCh38
NC_000010.10:g.64370108C>G , CM000672.1:g.64370108C>G GRCh37
NC_000010.9:g.64040114C>G NCBI36
NG_021209.1:g.241193C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647733.1:c.982-12754C>G ENSP00000502188.1:n.982-12754C>G
ENST00000395251.5:c.-184-33393C>G ENSP00000378672.1:n.-184-33393C>G
ENST00000410046.7:c.982-12754C>G ENSP00000387091.3:n.982-12754C>G
NM_199451.2:c.982-12754C>G NP_955523.1:n.982-12754C>G
NM_199452.3:c.-184-33393C>G NP_955524.3:n.-184-33393C>G
NM_199451.3:c.982-12754C>G NP_955523.1:n.982-12754C>G