Canonical Allele Identifier: CA14394661
Gene: ZBTB4 HGNC NCBI

Linked Data

dbSNP Id: rs9217

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7459769T>C , CM000679.2:g.7459769T>C GRCh38
NC_000017.10:g.7363088T>C , CM000679.1:g.7363088T>C GRCh37
NC_000017.9:g.7303812T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000380599.9:c.*2171A>G MANE Select ENSP00000369973.4:p.=
ENST00000311403.4:c.*2171A>G ENSP00000307858.4:p.=
ENST00000380599.8:c.*2171A>G ENSP00000369973.4:p.=
NM_001128833.1:c.*2170A>G NP_001122305.1:p.=
NM_020899.3:c.*2170A>G NP_065950.2:p.=
XM_006721563.2:c.*2171A>G XP_006721626.1:p.=
XM_006721564.1:c.*2171A>G XP_006721627.1:p.=
XM_011523972.1:c.*2171A>G XP_011522274.1:p.=
XM_006721563.3:c.*2171A>G XP_006721626.1:p.=
XM_006721564.2:c.*2171A>G XP_006721627.1:p.=
XM_011523972.2:c.*2171A>G XP_011522274.1:p.=
NM_001128833.2:c.*2171A>G MANE Select NP_001122305.1:p.=
NM_020899.4:c.*2171A>G NP_065950.2:p.=