Canonical Allele Identifier: CA1914566228
Gene: ZNF365 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62491999T= , CM000672.2:g.62491999T= GRCh38
NC_000010.10:g.64251758T= , CM000672.1:g.64251758T= GRCh37
NC_000010.9:g.63921764T= NCBI36
NG_021209.1:g.122843T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.981+32202T= ENSP00000502188.1:n.981+32202T=
ENST00000410046.7:c.981+32202T= ENSP00000387091.3:n.981+32202T=
NM_199451.2:c.981+32202T= NP_955523.1:n.981+32202T=
XM_017015937.2:c.981+32202T= XP_016871426.1:n.981+32202T=
NM_199451.3:c.981+32202T= NP_955523.1:n.981+32202T=