Canonical Allele Identifier: CA2245824331
Gene: ZBTB4 HGNC NCBI

Linked Data

dbSNP Id: rs2069990017

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7459647A>G , CM000679.2:g.7459647A>G GRCh38
NC_000017.10:g.7362966A>G , CM000679.1:g.7362966A>G GRCh37
NC_000017.9:g.7303690A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380599.9:c.*2293T>C MANE Select ENSP00000369973.4:n.*2293T>C
ENST00000311403.4:c.*2293T>C ENSP00000307858.4:n.*2293T>C
ENST00000380599.8:c.*2293T>C ENSP00000369973.4:n.*2293T>C
NM_001128833.1:c.*2292T>C NP_001122305.1:n.*2292T>C
NM_020899.3:c.*2292T>C NP_065950.2:n.*2292T>C
XM_006721563.2:c.*2293T>C XP_006721626.1:n.*2293T>C
XM_006721564.1:c.*2293T>C XP_006721627.1:n.*2293T>C
XM_011523972.1:c.*2293T>C XP_011522274.1:n.*2293T>C
XM_006721563.3:c.*2293T>C XP_006721626.1:n.*2293T>C
XM_006721564.2:c.*2293T>C XP_006721627.1:n.*2293T>C
XM_011523972.2:c.*2293T>C XP_011522274.1:n.*2293T>C
NM_001128833.2:c.*2293T>C MANE Select NP_001122305.1:n.*2293T>C
NM_020899.4:c.*2293T>C NP_065950.2:n.*2293T>C