Canonical Allele Identifier: CA667311425
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1477240023
MyVariant Identifiers: chr10:g.64380442A>T (hg19) chr10:g.62620682A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62620682A>T , CM000672.2:g.62620682A>T GRCh38
NC_000010.10:g.64380442A>T , CM000672.1:g.64380442A>T GRCh37
NC_000010.9:g.64050448A>T NCBI36
NG_021209.1:g.251527A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647733.1:c.982-2421A>T ENSP00000502188.1:n.982-2421A>T
ENST00000395251.5:c.-184-23060A>T ENSP00000378672.1:n.-184-23060A>T
ENST00000410046.7:c.982-2421A>T ENSP00000387091.3:n.982-2421A>T
NM_199451.2:c.982-2421A>T NP_955523.1:n.982-2421A>T
NM_199452.3:c.-184-23060A>T NP_955524.3:n.-184-23060A>T
NM_199451.3:c.982-2421A>T NP_955523.1:n.982-2421A>T
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