Canonical Allele Identifier: CA1914569554
Gene: ZNF365 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62501347C= , CM000672.2:g.62501347C= GRCh38
NC_000010.10:g.64261106C= , CM000672.1:g.64261106C= GRCh37
NC_000010.9:g.63931112C= NCBI36
NG_021209.1:g.132191C=

Transcript Alleles

HGVS Amino-acid change
ENST00000647733.1:c.981+41550C= ENSP00000502188.1:n.981+41550C=
ENST00000410046.7:c.981+41550C= ENSP00000387091.3:n.981+41550C=
NM_199451.2:c.981+41550C= NP_955523.1:n.981+41550C=
XM_017015937.2:c.981+41550C= XP_016871426.1:n.981+41550C=
NM_199451.3:c.981+41550C= NP_955523.1:n.981+41550C=