Canonical Allele Identifier: CA667276898
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1355528694
gnomAD v3: 10-62531576-T-C
gnomAD v4: 10-62531576-T-C
MyVariant Identifiers: chr10:g.64291335T>C (hg19) chr10:g.62531576T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62531576T>C , CM000672.2:g.62531576T>C GRCh38
NC_000010.10:g.64291335T>C , CM000672.1:g.64291335T>C GRCh37
NC_000010.9:g.63961341T>C NCBI36
NG_021209.1:g.162420T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.981+71779T>C ENSP00000502188.1:n.981+71779T>C
ENST00000395251.5:c.-185+10979T>C ENSP00000378672.1:n.-185+10979T>C
ENST00000410046.7:c.981+71779T>C ENSP00000387091.3:n.981+71779T>C
NM_199451.2:c.981+71779T>C NP_955523.1:n.981+71779T>C
NM_199452.3:c.-185+10979T>C NP_955524.3:n.-185+10979T>C
XM_017015937.2:c.982-12633T>C XP_016871426.1:n.982-12633T>C
NM_199451.3:c.981+71779T>C NP_955523.1:n.981+71779T>C
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