Canonical Allele Identifier: CA667311321
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1403568680

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62620503dup , CM000672.2:g.62620503dup GRCh38
NC_000010.10:g.64380263dup , CM000672.1:g.64380263dup GRCh37
NC_000010.9:g.64050269dup NCBI36
NG_021209.1:g.251348dup

Transcript Alleles

HGVS Amino-acid change
ENST00000647733.1:c.982-2600dup ENSP00000502188.1:n.982-2600dup
ENST00000395251.5:c.-184-23239dup ENSP00000378672.1:n.-184-23239dup
ENST00000410046.7:c.982-2600dup ENSP00000387091.3:n.982-2600dup
NM_199451.2:c.982-2600dup NP_955523.1:n.982-2600dup
NM_199452.3:c.-184-23239dup NP_955524.3:n.-184-23239dup
NM_199451.3:c.982-2600dup NP_955523.1:n.982-2600dup