Canonical Allele Identifier: CA1914624677
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1840163756

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62620422C>T , CM000672.2:g.62620422C>T GRCh38
NC_000010.10:g.64380182C>T , CM000672.1:g.64380182C>T GRCh37
NC_000010.9:g.64050188C>T NCBI36
NG_021209.1:g.251267C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.982-2681C>T ENSP00000502188.1:n.982-2681C>T
ENST00000395251.5:c.-184-23320C>T ENSP00000378672.1:n.-184-23320C>T
ENST00000410046.7:c.982-2681C>T ENSP00000387091.3:n.982-2681C>T
NM_199451.2:c.982-2681C>T NP_955523.1:n.982-2681C>T
NM_199452.3:c.-184-23320C>T NP_955524.3:n.-184-23320C>T
NM_199451.3:c.982-2681C>T NP_955523.1:n.982-2681C>T