Canonical Allele Identifier: CA667277195
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1342458944
gnomAD v3: 10-62531718-C-G
gnomAD v4: 10-62531718-C-G
MyVariant Identifiers: chr10:g.64291477C>G (hg19) chr10:g.62531718C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62531718C>G , CM000672.2:g.62531718C>G GRCh38
NC_000010.10:g.64291477C>G , CM000672.1:g.64291477C>G GRCh37
NC_000010.9:g.63961483C>G NCBI36
NG_021209.1:g.162562C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.981+71921C>G ENSP00000502188.1:n.981+71921C>G
ENST00000395251.5:c.-185+11121C>G ENSP00000378672.1:n.-185+11121C>G
ENST00000410046.7:c.981+71921C>G ENSP00000387091.3:n.981+71921C>G
NM_199451.2:c.981+71921C>G NP_955523.1:n.981+71921C>G
NM_199452.3:c.-185+11121C>G NP_955524.3:n.-185+11121C>G
XM_017015937.2:c.982-12491C>G XP_016871426.1:n.982-12491C>G
NM_199451.3:c.981+71921C>G NP_955523.1:n.981+71921C>G
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