Canonical Allele Identifier: CA929130006
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1840029867

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62610244G>A , CM000672.2:g.62610244G>A GRCh38
NC_000010.10:g.64370003G>A , CM000672.1:g.64370003G>A GRCh37
NC_000010.9:g.64040009G>A NCBI36
NG_021209.1:g.241088G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647733.1:c.982-12859G>A ENSP00000502188.1:n.982-12859G>A
ENST00000395251.5:c.-184-33498G>A ENSP00000378672.1:n.-184-33498G>A
ENST00000410046.7:c.982-12859G>A ENSP00000387091.3:n.982-12859G>A
NM_199451.2:c.982-12859G>A NP_955523.1:n.982-12859G>A
NM_199452.3:c.-184-33498G>A NP_955524.3:n.-184-33498G>A
NM_199451.3:c.982-12859G>A NP_955523.1:n.982-12859G>A