Canonical Allele Identifier: CA2327077599
Community Standard Title: NM_031218.4(ZNF93):c.227-7815T=
Gene: ZNF93 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.19925367T= , CM000681.2:g.19925367T= GRCh38
NC_000019.9:g.20036176T= , CM000681.1:g.20036176T= GRCh37
NC_000019.8:g.19897176T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_031218.4:c.227-7815T= MANE Select NP_112495.2:n.227-7815T=
ENST00000343769.6:c.227-7815T= MANE Select ENSP00000342002.4:n.227-7815T=
NM_031218.3:c.227-7815T= NP_112495.2:n.227-7815T=
ENST00000343769.5:c.227-7815T= ENSP00000342002.4:n.227-7815T=
ENST00000586021.5:c.227-734T= ENSP00000468563.1:n.227-734T=
ENST00000588146.1:c.35-7815T= ENSP00000467553.1:n.35-7815T=
ENST00000589903.1:n.422-1744T=
ENST00000591366.5:c.227-1744T= ENSP00000467652.1:n.227-1744T=
ENST00000592160.5:c.227-6641T= ENSP00000467377.1:n.227-6641T=
ENST00000592245.1:n.72+24328T=
XM_011528339.1:c.131-7815T= XP_011526641.1:n.131-7815T=