Canonical Allele Identifier: CA1914577441
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1838565811
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62518850A>T , CM000672.2:g.62518850A>T GRCh38
NC_000010.10:g.64278609A>T , CM000672.1:g.64278609A>T GRCh37
NC_000010.9:g.63948615A>T NCBI36
NG_021209.1:g.149694A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.981+59053A>T ENSP00000502188.1:n.981+59053A>T
ENST00000410046.7:c.981+59053A>T ENSP00000387091.3:n.981+59053A>T
NM_199451.2:c.981+59053A>T NP_955523.1:n.981+59053A>T
XM_017015937.2:c.982-25359A>T XP_016871426.1:n.982-25359A>T
NM_199451.3:c.981+59053A>T NP_955523.1:n.981+59053A>T
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