Canonical Allele Identifier: CA929114811
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1403195824
gnomAD v3: 10-62492094-T-C
gnomAD v4: 10-62492094-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62492094T>C , CM000672.2:g.62492094T>C GRCh38
NC_000010.10:g.64251853T>C , CM000672.1:g.64251853T>C GRCh37
NC_000010.9:g.63921859T>C NCBI36
NG_021209.1:g.122938T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647733.1:c.981+32297T>C ENSP00000502188.1:n.981+32297T>C
ENST00000410046.7:c.981+32297T>C ENSP00000387091.3:n.981+32297T>C
NM_199451.2:c.981+32297T>C NP_955523.1:n.981+32297T>C
XM_017015937.2:c.981+32297T>C XP_016871426.1:n.981+32297T>C
NM_199451.3:c.981+32297T>C NP_955523.1:n.981+32297T>C
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