Canonical Allele Identifier: CA208592186
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs976298014
gnomAD v3: 10-62528330-G-A
gnomAD v4: 10-62528330-G-A
MyVariant Identifiers: chr10:g.62528330G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62528330G>A , CM000672.2:g.62528330G>A GRCh38
NC_000010.10:g.64288089G>A , CM000672.1:g.64288089G>A GRCh37
NC_000010.9:g.63958095G>A NCBI36
NG_021209.1:g.159174G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647733.1:c.981+68533G>A ENSP00000502188.1:n.981+68533G>A
ENST00000395251.5:c.-185+7733G>A ENSP00000378672.1:n.-185+7733G>A
ENST00000410046.7:c.981+68533G>A ENSP00000387091.3:n.981+68533G>A
NM_199451.2:c.981+68533G>A NP_955523.1:n.981+68533G>A
NM_199452.3:c.-185+7733G>A NP_955524.3:n.-185+7733G>A
XM_017015937.2:c.982-15879G>A XP_016871426.1:n.982-15879G>A
NM_199451.3:c.981+68533G>A NP_955523.1:n.981+68533G>A
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