Canonical Allele Identifier: CA667311305
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1228273464
MyVariant Identifiers: chr10:g.64380222T>C (hg19) chr10:g.62620462T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62620462T>C , CM000672.2:g.62620462T>C GRCh38
NC_000010.10:g.64380222T>C , CM000672.1:g.64380222T>C GRCh37
NC_000010.9:g.64050228T>C NCBI36
NG_021209.1:g.251307T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.982-2641T>C ENSP00000502188.1:n.982-2641T>C
ENST00000395251.5:c.-184-23280T>C ENSP00000378672.1:n.-184-23280T>C
ENST00000410046.7:c.982-2641T>C ENSP00000387091.3:n.982-2641T>C
NM_199451.2:c.982-2641T>C NP_955523.1:n.982-2641T>C
NM_199452.3:c.-184-23280T>C NP_955524.3:n.-184-23280T>C
NM_199451.3:c.982-2641T>C NP_955523.1:n.982-2641T>C
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