Canonical Allele Identifier: CA594050450
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1392302662
gnomAD v2: 10-64391345-A-G
MyVariant Identifiers: chr10:g.64391345A>G (hg19) chr10:g.62631585A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62631585A>G , CM000672.2:g.62631585A>G GRCh38
NC_000010.10:g.64391345A>G , CM000672.1:g.64391345A>G GRCh37
NC_000010.9:g.64061351A>G NCBI36
NG_021209.1:g.262430A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.1129+8335A>G ENSP00000502188.1:n.1129+8335A>G
ENST00000395251.5:c.-184-12157A>G ENSP00000378672.1:n.-184-12157A>G
ENST00000410046.7:c.1129+8335A>G ENSP00000387091.3:n.1129+8335A>G
NM_199451.2:c.1129+8335A>G NP_955523.1:n.1129+8335A>G
NM_199452.3:c.-184-12157A>G NP_955524.3:n.-184-12157A>G
XR_946002.1:n.82-6462T>C
XR_946002.2:n.82-6462T>C
NM_199451.3:c.1129+8335A>G NP_955523.1:n.1129+8335A>G
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