Canonical Allele Identifier: CA1914551941
Gene: ZNF365 HGNC NCBI

Linked Data

dbSNP Id: rs1564599757
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.62463658A>G , CM000672.2:g.62463658A>G GRCh38
NC_000010.10:g.64223417A>G , CM000672.1:g.64223417A>G GRCh37
NC_000010.9:g.63893423A>G NCBI36
NG_021209.1:g.94502A>G
NG_021209.2:g.94467A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647733.1:c.981+3861A>G ENSP00000502188.1:n.981+3861A>G
ENST00000395255.7:c.981+3861A>G ENSP00000378675.3:n.981+3861A>G
ENST00000410046.7:c.981+3861A>G ENSP00000387091.3:n.981+3861A>G
NM_199450.2:c.981+3861A>G NP_955522.1:n.981+3861A>G
NM_199451.2:c.981+3861A>G NP_955523.1:n.981+3861A>G
XM_017015937.2:c.981+3861A>G XP_016871426.1:n.981+3861A>G
NM_199451.3:c.981+3861A>G NP_955523.1:n.981+3861A>G
NM_199450.3:c.981+3861A>G NP_955522.1:n.981+3861A>G
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