Canonical Allele Identifier: CA594035852
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1406233331
gnomAD v2: 10-64291419-A-T
gnomAD v3: 10-62531660-A-T
gnomAD v4: 10-62531660-A-T
MyVariant Identifiers: chr10:g.64291419A>T (hg19) chr10:g.62531660A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62531660A>T , CM000672.2:g.62531660A>T GRCh38
NC_000010.10:g.64291419A>T , CM000672.1:g.64291419A>T GRCh37
NC_000010.9:g.63961425A>T NCBI36
NG_021209.1:g.162504A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.981+71863A>T ENSP00000502188.1:n.981+71863A>T
ENST00000395251.5:c.-185+11063A>T ENSP00000378672.1:n.-185+11063A>T
ENST00000410046.7:c.981+71863A>T ENSP00000387091.3:n.981+71863A>T
NM_199451.2:c.981+71863A>T NP_955523.1:n.981+71863A>T
NM_199452.3:c.-185+11063A>T NP_955524.3:n.-185+11063A>T
XM_017015937.2:c.982-12549A>T XP_016871426.1:n.982-12549A>T
NM_199451.3:c.981+71863A>T NP_955523.1:n.981+71863A>T
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