Canonical Allele Identifier: CA1914620042
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1840030810

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62610323A>C , CM000672.2:g.62610323A>C GRCh38
NC_000010.10:g.64370082A>C , CM000672.1:g.64370082A>C GRCh37
NC_000010.9:g.64040088A>C NCBI36
NG_021209.1:g.241167A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.982-12780A>C ENSP00000502188.1:n.982-12780A>C
ENST00000395251.5:c.-184-33419A>C ENSP00000378672.1:n.-184-33419A>C
ENST00000410046.7:c.982-12780A>C ENSP00000387091.3:n.982-12780A>C
NM_199451.2:c.982-12780A>C NP_955523.1:n.982-12780A>C
NM_199452.3:c.-184-33419A>C NP_955524.3:n.-184-33419A>C
NM_199451.3:c.982-12780A>C NP_955523.1:n.982-12780A>C