Canonical Allele Identifier: CA1914569627
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1564614276

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62501478A>T , CM000672.2:g.62501478A>T GRCh38
NC_000010.10:g.64261237A>T , CM000672.1:g.64261237A>T GRCh37
NC_000010.9:g.63931243A>T NCBI36
NG_021209.1:g.132322A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647733.1:c.981+41681A>T ENSP00000502188.1:n.981+41681A>T
ENST00000410046.7:c.981+41681A>T ENSP00000387091.3:n.981+41681A>T
NM_199451.2:c.981+41681A>T NP_955523.1:n.981+41681A>T
XM_017015937.2:c.981+41681A>T XP_016871426.1:n.981+41681A>T
NM_199451.3:c.981+41681A>T NP_955523.1:n.981+41681A>T