Canonical Allele Identifier: CA1914583886
Gene: ZNF365 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62531286T= , CM000672.2:g.62531286T= GRCh38
NC_000010.10:g.64291045T= , CM000672.1:g.64291045T= GRCh37
NC_000010.9:g.63961051T= NCBI36
NG_021209.1:g.162130T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.981+71489T= ENSP00000502188.1:n.981+71489T=
ENST00000395251.5:c.-185+10689T= ENSP00000378672.1:n.-185+10689T=
ENST00000410046.7:c.981+71489T= ENSP00000387091.3:n.981+71489T=
NM_199451.2:c.981+71489T= NP_955523.1:n.981+71489T=
NM_199452.3:c.-185+10689T= NP_955524.3:n.-185+10689T=
XM_017015937.2:c.982-12923T= XP_016871426.1:n.982-12923T=
NM_199451.3:c.981+71489T= NP_955523.1:n.981+71489T=