Canonical Allele Identifier: CA774959485

Gene: ZBTB4

Linked Data

• dbSNP Id: rs1250010488
• gnomAD v3: 17-7459658-A-G
• gnomAD v4: 17-7459658-A-G
• MyVariant Identifiers: chr17:g.7362977A>G (hg19) ; chr17:g.7459658A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7459658A>G , CM000679.2:g.7459658A>G	GRCh38
NC_000017.10:g.7362977A>G , CM000679.1:g.7362977A>G	GRCh37
NC_000017.9:g.7303701A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000380599.9:c.*2282T>C MANE Select	ENSP00000369973.4:n.*2282T>C
ENST00000311403.4:c.*2282T>C	ENSP00000307858.4:n.*2282T>C
ENST00000380599.8:c.*2282T>C	ENSP00000369973.4:n.*2282T>C
NM_001128833.1:c.*2281T>C	NP_001122305.1:n.*2281T>C
NM_020899.3:c.*2281T>C	NP_065950.2:n.*2281T>C
XM_006721563.2:c.*2282T>C	XP_006721626.1:n.*2282T>C
XM_006721564.1:c.*2282T>C	XP_006721627.1:n.*2282T>C
XM_011523972.1:c.*2282T>C	XP_011522274.1:n.*2282T>C
XM_006721563.3:c.*2282T>C	XP_006721626.1:n.*2282T>C
XM_006721564.2:c.*2282T>C	XP_006721627.1:n.*2282T>C
XM_011523972.2:c.*2282T>C	XP_011522274.1:n.*2282T>C
NM_001128833.2:c.*2282T>C MANE Select	NP_001122305.1:n.*2282T>C
NM_020899.4:c.*2282T>C	NP_065950.2:n.*2282T>C