Canonical Allele Identifier: CA287435883

Gene: ZBTB4

Linked Data

• dbSNP Id: rs932857011
• gnomAD v2: 17-7363059-C-T
• gnomAD v3: 17-7459740-C-T
• gnomAD v4: 17-7459740-C-T
• MyVariant Identifiers: chr17:g.7363059C>T (hg19) ; chr17:g.7459740C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7459740C>T , CM000679.2:g.7459740C>T	GRCh38
NC_000017.10:g.7363059C>T , CM000679.1:g.7363059C>T	GRCh37
NC_000017.9:g.7303783C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000380599.9:c.*2200G>A MANE Select	ENSP00000369973.4:n.*2200G>A
ENST00000311403.4:c.*2200G>A	ENSP00000307858.4:n.*2200G>A
ENST00000380599.8:c.*2200G>A	ENSP00000369973.4:n.*2200G>A
NM_001128833.1:c.*2199G>A	NP_001122305.1:n.*2199G>A
NM_020899.3:c.*2199G>A	NP_065950.2:n.*2199G>A
XM_006721563.2:c.*2200G>A	XP_006721626.1:n.*2200G>A
XM_006721564.1:c.*2200G>A	XP_006721627.1:n.*2200G>A
XM_011523972.1:c.*2200G>A	XP_011522274.1:n.*2200G>A
XM_006721563.3:c.*2200G>A	XP_006721626.1:n.*2200G>A
XM_006721564.2:c.*2200G>A	XP_006721627.1:n.*2200G>A
XM_011523972.2:c.*2200G>A	XP_011522274.1:n.*2200G>A
NM_001128833.2:c.*2200G>A MANE Select	NP_001122305.1:n.*2200G>A
NM_020899.4:c.*2200G>A	NP_065950.2:n.*2200G>A