Canonical Allele Identifier: CA2245824385
Gene: ZBTB4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7459759C= , CM000679.2:g.7459759C= GRCh38
NC_000017.10:g.7363078C= , CM000679.1:g.7363078C= GRCh37
NC_000017.9:g.7303802C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000380599.9:c.*2181G= MANE Select ENSP00000369973.4:n.*2181G=
ENST00000311403.4:c.*2181G= ENSP00000307858.4:n.*2181G=
ENST00000380599.8:c.*2181G= ENSP00000369973.4:n.*2181G=
NM_001128833.1:c.*2180G= NP_001122305.1:n.*2180G=
NM_020899.3:c.*2180G= NP_065950.2:n.*2180G=
XM_006721563.2:c.*2181G= XP_006721626.1:n.*2181G=
XM_006721564.1:c.*2181G= XP_006721627.1:n.*2181G=
XM_011523972.1:c.*2181G= XP_011522274.1:n.*2181G=
XM_006721563.3:c.*2181G= XP_006721626.1:n.*2181G=
XM_006721564.2:c.*2181G= XP_006721627.1:n.*2181G=
XM_011523972.2:c.*2181G= XP_011522274.1:n.*2181G=
NM_001128833.2:c.*2181G= MANE Select NP_001122305.1:n.*2181G=
NM_020899.4:c.*2181G= NP_065950.2:n.*2181G=