Canonical Allele Identifier: CA14394661

Gene: ZBTB4

Linked Data

• dbSNP Id: rs9217
• gnomAD v2: 17-7363088-T-C
• gnomAD v3: 17-7459769-T-C
• gnomAD v4: 17-7459769-T-C
• MyVariant Identifiers: chr17:g.7363088T>C (hg19) ; chr17:g.7459769T>C (hg38)

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:n.*2171A>G
ENST00000311403.4:c.*2171A>G	ENSP00000307858.4:n.*2171A>G
ENST00000380599.8:c.*2171A>G	ENSP00000369973.4:n.*2171A>G
NM_001128833.1:c.*2170A>G	NP_001122305.1:n.*2170A>G
NM_020899.3:c.*2170A>G	NP_065950.2:n.*2170A>G
XM_006721563.2:c.*2171A>G	XP_006721626.1:n.*2171A>G
XM_006721564.1:c.*2171A>G	XP_006721627.1:n.*2171A>G
XM_011523972.1:c.*2171A>G	XP_011522274.1:n.*2171A>G
XM_006721563.3:c.*2171A>G	XP_006721626.1:n.*2171A>G
XM_006721564.2:c.*2171A>G	XP_006721627.1:n.*2171A>G
XM_011523972.2:c.*2171A>G	XP_011522274.1:n.*2171A>G
NM_001128833.2:c.*2171A>G MANE Select	NP_001122305.1:n.*2171A>G
NM_020899.4:c.*2171A>G	NP_065950.2:n.*2171A>G