Canonical Allele Identifier: CA208589089
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs886104749

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62501480dup , CM000672.2:g.62501480dup GRCh38
NC_000010.10:g.64261239dup , CM000672.1:g.64261239dup GRCh37
NC_000010.9:g.63931245dup NCBI36
NG_021209.1:g.132324dup

Transcript Alleles

HGVS Amino-acid change
ENST00000647733.1:c.981+41683dup ENSP00000502188.1:n.981+41683dup
ENST00000410046.7:c.981+41683dup ENSP00000387091.3:n.981+41683dup
NM_199451.2:c.981+41683dup NP_955523.1:n.981+41683dup
XM_017015937.2:c.981+41683dup XP_016871426.1:n.981+41683dup
NM_199451.3:c.981+41683dup NP_955523.1:n.981+41683dup