Canonical Allele Identifier: CA594035152
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1365674515
gnomAD v2: 10-64288050-C-G
MyVariant Identifiers: chr10:g.64288050C>G (hg19) chr10:g.62528291C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62528291C>G , CM000672.2:g.62528291C>G GRCh38
NC_000010.10:g.64288050C>G , CM000672.1:g.64288050C>G GRCh37
NC_000010.9:g.63958056C>G NCBI36
NG_021209.1:g.159135C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647733.1:c.981+68494C>G ENSP00000502188.1:n.981+68494C>G
ENST00000395251.5:c.-185+7694C>G ENSP00000378672.1:n.-185+7694C>G
ENST00000410046.7:c.981+68494C>G ENSP00000387091.3:n.981+68494C>G
NM_199451.2:c.981+68494C>G NP_955523.1:n.981+68494C>G
NM_199452.3:c.-185+7694C>G NP_955524.3:n.-185+7694C>G
XM_017015937.2:c.982-15918C>G XP_016871426.1:n.982-15918C>G
NM_199451.3:c.981+68494C>G NP_955523.1:n.981+68494C>G
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