Canonical Allele Identifier: CA2722057857
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1838746437

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62528588C>T , CM000672.2:g.62528588C>T GRCh38
NC_000010.10:g.64288347C>T , CM000672.1:g.64288347C>T GRCh37
NC_000010.9:g.63958353C>T NCBI36
NG_021209.1:g.159432C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.981+68791C>T ENSP00000502188.1:n.981+68791C>T
ENST00000395251.5:c.-185+7991C>T ENSP00000378672.1:n.-185+7991C>T
ENST00000410046.7:c.981+68791C>T ENSP00000387091.3:n.981+68791C>T
NM_199451.2:c.981+68791C>T NP_955523.1:n.981+68791C>T
NM_199452.3:c.-185+7991C>T NP_955524.3:n.-185+7991C>T
XM_017015937.2:c.982-15621C>T XP_016871426.1:n.982-15621C>T
NM_199451.3:c.981+68791C>T NP_955523.1:n.981+68791C>T