Canonical Allele Identifier: CA208592213
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs372502477
gnomAD v2: 10-64288397-G-GGA
gnomAD v3: 10-62528638-G-GGA
gnomAD v4: 10-62528638-G-GGA
MyVariant Identifiers: chr10:g.64288397_64288398insGA (hg19) chr10:g.64288398_64288399delinsGAAA (hg19) chr10:g.62528638_62528639insGA (hg38) chr10:g.62528639_62528640delinsGAAA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62528638_62528639insGA , CM000672.2:g.62528638_62528639insGA GRCh38
NC_000010.10:g.64288397_64288398insGA , CM000672.1:g.64288397_64288398insGA GRCh37
NC_000010.9:g.63958403_63958404insGA NCBI36
NG_021209.1:g.159482_159483insGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.981+68841_981+68842insGA ENSP00000502188.1:n.981+68841_981+68842insGA
ENST00000395251.5:c.-185+8041_-185+8042insGA ENSP00000378672.1:n.-185+8041_-185+8042insGA
ENST00000410046.7:c.981+68841_981+68842insGA ENSP00000387091.3:n.981+68841_981+68842insGA
NM_199451.2:c.981+68841_981+68842insGA NP_955523.1:n.981+68841_981+68842insGA
NM_199452.3:c.-185+8041_-185+8042insGA NP_955524.3:n.-185+8041_-185+8042insGA
XM_017015937.2:c.982-15571_982-15570insGA XP_016871426.1:n.982-15571_982-15570insGA
NM_199451.3:c.981+68841_981+68842insGA NP_955523.1:n.981+68841_981+68842insGA
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