Canonical Allele Identifier: CA208592498
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs11478176
gnomAD v2: 10-64291083-AC-A
gnomAD v3: 10-62531324-AC-A
gnomAD v4: 10-62531324-AC-A
MyVariant Identifiers: chr10:g.64291084del (hg19) chr10:g.62531325del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62531325del , CM000672.2:g.62531325del GRCh38
NC_000010.10:g.64291084del , CM000672.1:g.64291084del GRCh37
NC_000010.9:g.63961090del NCBI36
NG_021209.1:g.162169del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.981+71528del ENSP00000502188.1:n.981+71528del
ENST00000395251.5:c.-185+10728del ENSP00000378672.1:n.-185+10728del
ENST00000410046.7:c.981+71528del ENSP00000387091.3:n.981+71528del
NM_199451.2:c.981+71528del NP_955523.1:n.981+71528del
NM_199452.3:c.-185+10728del NP_955524.3:n.-185+10728del
XM_017015937.2:c.982-12884del XP_016871426.1:n.982-12884del
NM_199451.3:c.981+71528del NP_955523.1:n.981+71528del
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