Canonical Allele Identifier: CA14685633
Gene: ZNF93 HGNC NCBI

Linked Data

dbSNP Id: rs10411195

Genomic Alleles

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

Transcript Alleles

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