Canonical Allele Identifier: CA929114799
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1841380514
gnomAD v3: 10-62491971-C-CT
gnomAD v4: 10-62491971-C-CT
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62491972dup , CM000672.2:g.62491972dup GRCh38
NC_000010.10:g.64251731dup , CM000672.1:g.64251731dup GRCh37
NC_000010.9:g.63921737dup NCBI36
NG_021209.1:g.122816dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.981+32175dup ENSP00000502188.1:n.981+32175dup
ENST00000410046.7:c.981+32175dup ENSP00000387091.3:n.981+32175dup
NM_199451.2:c.981+32175dup NP_955523.1:n.981+32175dup
XM_017015937.2:c.981+32175dup XP_016871426.1:n.981+32175dup
NM_199451.3:c.981+32175dup NP_955523.1:n.981+32175dup
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