Canonical Allele Identifier: CA929133804
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1840166028

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62620583G>A , CM000672.2:g.62620583G>A GRCh38
NC_000010.10:g.64380343G>A , CM000672.1:g.64380343G>A GRCh37
NC_000010.9:g.64050349G>A NCBI36
NG_021209.1:g.251428G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647733.1:c.982-2520G>A ENSP00000502188.1:n.982-2520G>A
ENST00000395251.5:c.-184-23159G>A ENSP00000378672.1:n.-184-23159G>A
ENST00000410046.7:c.982-2520G>A ENSP00000387091.3:n.982-2520G>A
NM_199451.2:c.982-2520G>A NP_955523.1:n.982-2520G>A
NM_199452.3:c.-184-23159G>A NP_955524.3:n.-184-23159G>A
NM_199451.3:c.982-2520G>A NP_955523.1:n.982-2520G>A