Canonical Allele Identifier: CA929120467
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1838793873
gnomAD v3: 10-62531261-A-G
gnomAD v4: 10-62531261-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62531261A>G , CM000672.2:g.62531261A>G GRCh38
NC_000010.10:g.64291020A>G , CM000672.1:g.64291020A>G GRCh37
NC_000010.9:g.63961026A>G NCBI36
NG_021209.1:g.162105A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.981+71464A>G ENSP00000502188.1:n.981+71464A>G
ENST00000395251.5:c.-185+10664A>G ENSP00000378672.1:n.-185+10664A>G
ENST00000410046.7:c.981+71464A>G ENSP00000387091.3:n.981+71464A>G
NM_199451.2:c.981+71464A>G NP_955523.1:n.981+71464A>G
NM_199452.3:c.-185+10664A>G NP_955524.3:n.-185+10664A>G
XM_017015937.2:c.982-12948A>G XP_016871426.1:n.982-12948A>G
NM_199451.3:c.981+71464A>G NP_955523.1:n.981+71464A>G
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