Canonical Allele Identifier: CA929120566
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1838800726

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62531555G>T , CM000672.2:g.62531555G>T GRCh38
NC_000010.10:g.64291314G>T , CM000672.1:g.64291314G>T GRCh37
NC_000010.9:g.63961320G>T NCBI36
NG_021209.1:g.162399G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647733.1:c.981+71758G>T ENSP00000502188.1:n.981+71758G>T
ENST00000395251.5:c.-185+10958G>T ENSP00000378672.1:n.-185+10958G>T
ENST00000410046.7:c.981+71758G>T ENSP00000387091.3:n.981+71758G>T
NM_199451.2:c.981+71758G>T NP_955523.1:n.981+71758G>T
NM_199452.3:c.-185+10958G>T NP_955524.3:n.-185+10958G>T
XM_017015937.2:c.982-12654G>T XP_016871426.1:n.982-12654G>T
NM_199451.3:c.981+71758G>T NP_955523.1:n.981+71758G>T