Canonical Allele Identifier: CA1914582493
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1838742550

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62528341T>C , CM000672.2:g.62528341T>C GRCh38
NC_000010.10:g.64288100T>C , CM000672.1:g.64288100T>C GRCh37
NC_000010.9:g.63958106T>C NCBI36
NG_021209.1:g.159185T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647733.1:c.981+68544T>C ENSP00000502188.1:n.981+68544T>C
ENST00000395251.5:c.-185+7744T>C ENSP00000378672.1:n.-185+7744T>C
ENST00000410046.7:c.981+68544T>C ENSP00000387091.3:n.981+68544T>C
NM_199451.2:c.981+68544T>C NP_955523.1:n.981+68544T>C
NM_199452.3:c.-185+7744T>C NP_955524.3:n.-185+7744T>C
XM_017015937.2:c.982-15868T>C XP_016871426.1:n.982-15868T>C
NM_199451.3:c.981+68544T>C NP_955523.1:n.981+68544T>C