Canonical Allele Identifier: CA287435889

Gene: ZBTB4

Linked Data

• dbSNP Id: rs533486632
• gnomAD v2: 17-7363069-G-A
• gnomAD v3: 17-7459750-G-A
• gnomAD v4: 17-7459750-G-A
• MyVariant Identifiers: chr17:g.7363069G>A (hg19) ; chr17:g.7459750G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7459750G>A , CM000679.2:g.7459750G>A	GRCh38
NC_000017.10:g.7363069G>A , CM000679.1:g.7363069G>A	GRCh37
NC_000017.9:g.7303793G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000380599.9:c.*2190C>T MANE Select	ENSP00000369973.4:n.*2190C>T
ENST00000311403.4:c.*2190C>T	ENSP00000307858.4:n.*2190C>T
ENST00000380599.8:c.*2190C>T	ENSP00000369973.4:n.*2190C>T
NM_001128833.1:c.*2189C>T	NP_001122305.1:n.*2189C>T
NM_020899.3:c.*2189C>T	NP_065950.2:n.*2189C>T
XM_006721563.2:c.*2190C>T	XP_006721626.1:n.*2190C>T
XM_006721564.1:c.*2190C>T	XP_006721627.1:n.*2190C>T
XM_011523972.1:c.*2190C>T	XP_011522274.1:n.*2190C>T
XM_006721563.3:c.*2190C>T	XP_006721626.1:n.*2190C>T
XM_006721564.2:c.*2190C>T	XP_006721627.1:n.*2190C>T
XM_011523972.2:c.*2190C>T	XP_011522274.1:n.*2190C>T
NM_001128833.2:c.*2190C>T MANE Select	NP_001122305.1:n.*2190C>T
NM_020899.4:c.*2190C>T	NP_065950.2:n.*2190C>T