Canonical Allele Identifier: CA667276957
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1239033586
gnomAD v3: 10-62531595-C-A
gnomAD v4: 10-62531595-C-A
MyVariant Identifiers: chr10:g.64291354C>A (hg19) chr10:g.62531595C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62531595C>A , CM000672.2:g.62531595C>A GRCh38
NC_000010.10:g.64291354C>A , CM000672.1:g.64291354C>A GRCh37
NC_000010.9:g.63961360C>A NCBI36
NG_021209.1:g.162439C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.981+71798C>A ENSP00000502188.1:n.981+71798C>A
ENST00000395251.5:c.-185+10998C>A ENSP00000378672.1:n.-185+10998C>A
ENST00000410046.7:c.981+71798C>A ENSP00000387091.3:n.981+71798C>A
NM_199451.2:c.981+71798C>A NP_955523.1:n.981+71798C>A
NM_199452.3:c.-185+10998C>A NP_955524.3:n.-185+10998C>A
XM_017015937.2:c.982-12614C>A XP_016871426.1:n.982-12614C>A
NM_199451.3:c.981+71798C>A NP_955523.1:n.981+71798C>A
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