Canonical Allele Identifier: CA667306025
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1300066175
MyVariant Identifiers: chr10:g.64369950G>C (hg19) chr10:g.62610191G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62610191G>C , CM000672.2:g.62610191G>C GRCh38
NC_000010.10:g.64369950G>C , CM000672.1:g.64369950G>C GRCh37
NC_000010.9:g.64039956G>C NCBI36
NG_021209.1:g.241035G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647733.1:c.982-12912G>C ENSP00000502188.1:n.982-12912G>C
ENST00000395251.5:c.-184-33551G>C ENSP00000378672.1:n.-184-33551G>C
ENST00000410046.7:c.982-12912G>C ENSP00000387091.3:n.982-12912G>C
NM_199451.2:c.982-12912G>C NP_955523.1:n.982-12912G>C
NM_199452.3:c.-184-33551G>C NP_955524.3:n.-184-33551G>C
NM_199451.3:c.982-12912G>C NP_955523.1:n.982-12912G>C
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