Canonical Allele Identifier: CA929119521
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1588978582
gnomAD v3: 10-62528599-T-C
gnomAD v4: 10-62528599-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62528599T>C , CM000672.2:g.62528599T>C GRCh38
NC_000010.10:g.64288358T>C , CM000672.1:g.64288358T>C GRCh37
NC_000010.9:g.63958364T>C NCBI36
NG_021209.1:g.159443T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647733.1:c.981+68802T>C ENSP00000502188.1:n.981+68802T>C
ENST00000395251.5:c.-185+8002T>C ENSP00000378672.1:n.-185+8002T>C
ENST00000410046.7:c.981+68802T>C ENSP00000387091.3:n.981+68802T>C
NM_199451.2:c.981+68802T>C NP_955523.1:n.981+68802T>C
NM_199452.3:c.-185+8002T>C NP_955524.3:n.-185+8002T>C
XM_017015937.2:c.982-15610T>C XP_016871426.1:n.982-15610T>C
NM_199451.3:c.981+68802T>C NP_955523.1:n.981+68802T>C
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