Canonical Allele Identifier: CA13267750
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs10995190

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62518923G>A , CM000672.2:g.62518923G>A GRCh38
NC_000010.10:g.64278682G>A , CM000672.1:g.64278682G>A GRCh37
NC_000010.9:g.63948688G>A NCBI36
NG_021209.1:g.149767G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647733.1:c.981+59126G>A ENSP00000502188.1:p.=
ENST00000410046.7:c.981+59126G>A ENSP00000387091.3:p.=
NM_199451.2:c.981+59126G>A NP_955523.1:p.=
XM_017015937.2:c.982-25286G>A XP_016871426.1:p.=
NM_199451.3:c.981+59126G>A NP_955523.1:p.=