Canonical Allele Identifier: CA208592522
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs558406152
gnomAD v2: 10-64291199-C-CA
gnomAD v3: 10-62531440-C-CA
gnomAD v4: 10-62531440-C-CA
MyVariant Identifiers: chr10:g.64291199_64291200insA (hg19) chr10:g.62531440_62531441insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62531447dup , CM000672.2:g.62531447dup GRCh38
NC_000010.10:g.64291206dup , CM000672.1:g.64291206dup GRCh37
NC_000010.9:g.63961212dup NCBI36
NG_021209.1:g.162291dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.981+71650dup ENSP00000502188.1:n.981+71650dup
ENST00000395251.5:c.-185+10850dup ENSP00000378672.1:n.-185+10850dup
ENST00000410046.7:c.981+71650dup ENSP00000387091.3:n.981+71650dup
NM_199451.2:c.981+71650dup NP_955523.1:n.981+71650dup
NM_199452.3:c.-185+10850dup NP_955524.3:n.-185+10850dup
XM_017015937.2:c.982-12762dup XP_016871426.1:n.982-12762dup
NM_199451.3:c.981+71650dup NP_955523.1:n.981+71650dup
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