Canonical Allele Identifier: CA594050448
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1423666812
gnomAD v2: 10-64391298-C-T
gnomAD v3: 10-62631538-C-T
gnomAD v4: 10-62631538-C-T
MyVariant Identifiers: chr10:g.64391298C>T (hg19) chr10:g.62631538C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62631538C>T , CM000672.2:g.62631538C>T GRCh38
NC_000010.10:g.64391298C>T , CM000672.1:g.64391298C>T GRCh37
NC_000010.9:g.64061304C>T NCBI36
NG_021209.1:g.262383C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647733.1:c.1129+8288C>T ENSP00000502188.1:n.1129+8288C>T
ENST00000395251.5:c.-184-12204C>T ENSP00000378672.1:n.-184-12204C>T
ENST00000410046.7:c.1129+8288C>T ENSP00000387091.3:n.1129+8288C>T
NM_199451.2:c.1129+8288C>T NP_955523.1:n.1129+8288C>T
NM_199452.3:c.-184-12204C>T NP_955524.3:n.-184-12204C>T
XR_946002.1:n.82-6415G>A
XR_946002.2:n.82-6415G>A
NM_199451.3:c.1129+8288C>T NP_955523.1:n.1129+8288C>T
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