Canonical Allele Identifier: CA929118359
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1838570372

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62519064del , CM000672.2:g.62519064del GRCh38
NC_000010.10:g.64278823del , CM000672.1:g.64278823del GRCh37
NC_000010.9:g.63948829del NCBI36
NG_021209.1:g.149908del

Transcript Alleles

HGVS Amino-acid change
ENST00000647733.1:c.981+59267del ENSP00000502188.1:n.981+59267del
ENST00000410046.7:c.981+59267del ENSP00000387091.3:n.981+59267del
NM_199451.2:c.981+59267del NP_955523.1:n.981+59267del
XM_017015937.2:c.982-25145del XP_016871426.1:n.982-25145del
NM_199451.3:c.981+59267del NP_955523.1:n.981+59267del