Canonical Allele Identifier: CA5516795
Gene: ZNF365 HGNC NCBI
MyVariant.info:
GRCh38 chr10:g.62655424A>G
GRCh37 chr10:g.64415184A>G
Revel Score:
ENST00000395251 0.039
gnomAD v2:
10:64415184 A / G
gnomAD v3:
10:62655424 A / G
gnomAD v4:
chr10-62655424-A-G
Joint Max Group AF 0.94601474 (AFR)
Genomes Max Group AF 0.94200187 (AFR)
Exomes Max Group AF 0.94559576 (AFR)
dbSNP:
7076156
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62655424A>G , CM000672.2:g.62655424A>G GRCh38
NC_000010.10:g.64415184A>G , CM000672.1:g.64415184A>G GRCh37
NC_000010.9:g.64085190A>G NCBI36
NG_021209.1:g.286269A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.1130-972A>G ENSP00000502188.1:n.1130-972A>G
ENST00000344640.7:c.126+494A>G ENSP00000345300.3:n.126+494A>G
ENST00000373784.6:c.126+494A>G ENSP00000362889.2:n.126+494A>G
ENST00000395249.5:c.39-10705A>G ENSP00000378670.1:n.39-10705A>G
ENST00000395251.5:c.184A>G ENSP00000378672.1:p.Thr62Ala
ENST00000410046.7:c.1130-972A>G ENSP00000387091.3:n.1130-972A>G
ENST00000461412.1:n.239A>G
ENST00000614806.1:c.184A>G ENSP00000481372.1:p.Thr62Ala
NM_199451.2:c.1130-972A>G NP_955523.1:n.1130-972A>G
XM_011539530.1:c.340A>G XP_011537832.1:p.Thr114Ala
XM_011539531.1:c.340A>G XP_011537833.1:p.Thr114Ala
XM_011539532.1:c.184A>G XP_011537834.1:p.Thr62Ala
XM_011539533.1:c.340A>G XP_011537835.1:p.Thr114Ala
XR_946002.1:n.81+2T>C
XM_017015938.1:c.340A>G XP_016871427.1:p.Thr114Ala
XM_017015939.1:c.340A>G XP_016871428.1:p.Thr114Ala
XM_017015940.1:c.184A>G XP_016871429.1:p.Thr62Ala
XM_017015941.1:c.340A>G XP_016871430.1:p.Thr114Ala
XR_946002.2:n.81+2T>C
NM_199451.3:c.1130-972A>G NP_955523.1:n.1130-972A>G
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