Canonical Allele Identifier: CA14535245
Gene: ZBTB7C HGNC NCBI

Linked Data

dbSNP Id: rs1944582
gnomAD v2: 18-45815417-A-G
gnomAD v3: 18-48289046-A-G
gnomAD v4: 18-48289046-A-G
MyVariant Identifiers: chr18:g.45815417A>G (hg19) chr18:g.48289046A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.48289046A>G , CM000680.2:g.48289046A>G GRCh38
NC_000018.9:g.45815417A>G , CM000680.1:g.45815417A>G GRCh37
NC_000018.8:g.44069415A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000590800.6:c.-79+49128T>C MANE Select ENSP00000467877.1:n.-79+49128T>C
ENST00000585404.5:c.-308+49128T>C ENSP00000464724.1:n.-308+49128T>C
ENST00000586525.5:c.-205-103051T>C ENSP00000468537.1:n.-205-103051T>C
ENST00000586743.5:c.-274+49128T>C ENSP00000466006.1:n.-274+49128T>C
ENST00000587107.5:c.-338+49128T>C ENSP00000465760.1:n.-338+49128T>C
ENST00000588028.1:c.-208+49128T>C ENSP00000468152.1:n.-208+49128T>C
ENST00000588053.5:c.-256+49128T>C ENSP00000466088.1:n.-256+49128T>C
ENST00000588149.5:c.-211+49128T>C ENSP00000468814.1:n.-211+49128T>C
ENST00000588566.5:c.-79+49128T>C ENSP00000467456.1:n.-79+49128T>C
ENST00000588970.5:c.-230+49128T>C ENSP00000468502.1:n.-230+49128T>C
ENST00000589077.5:c.-170+49128T>C ENSP00000467147.1:n.-170+49128T>C
ENST00000589170.5:c.-343-36748T>C ENSP00000467338.1:n.-343-36748T>C
ENST00000589194.5:c.-359+49128T>C ENSP00000468019.1:n.-359+49128T>C
ENST00000589619.5:c.-278+49128T>C ENSP00000468659.1:n.-278+49128T>C
ENST00000590178.5:c.-206+49128T>C ENSP00000465160.1:n.-206+49128T>C
ENST00000590374.5:c.-334+49128T>C ENSP00000465494.1:n.-334+49128T>C
ENST00000590800.5:c.-79+49128T>C ENSP00000467877.1:n.-79+49128T>C
ENST00000590855.5:c.-206+49128T>C ENSP00000468306.1:n.-206+49128T>C
ENST00000591279.5:c.-78-103051T>C ENSP00000465265.1:n.-78-103051T>C
ENST00000591405.5:c.-79+49128T>C ENSP00000467758.1:n.-79+49128T>C
ENST00000591526.5:c.-252+49128T>C ENSP00000468752.1:n.-252+49128T>C
ENST00000592387.5:c.-255-103051T>C ENSP00000465835.1:n.-255-103051T>C
ENST00000592656.5:c.-388+49128T>C ENSP00000468087.1:n.-388+49128T>C
ENST00000593159.5:c.-270+49128T>C ENSP00000465832.1:n.-270+49128T>C
XM_005258227.2:c.-79+49128T>C XP_005258284.1:n.-79+49128T>C
XM_005258229.3:c.-78-103051T>C XP_005258286.1:n.-78-103051T>C
XM_011525861.1:c.-187+49128T>C XP_011524163.1:n.-187+49128T>C
XM_011525863.1:c.-179+49128T>C XP_011524165.1:n.-179+49128T>C
XM_011525864.1:c.-179+49128T>C XP_011524166.1:n.-179+49128T>C
XM_011525865.1:c.-175+49128T>C XP_011524167.1:n.-175+49128T>C
XM_011525867.1:c.-178-103051T>C XP_011524169.1:n.-178-103051T>C
XM_011525870.1:c.-78-103051T>C XP_011524172.1:n.-78-103051T>C
NM_001318841.1:c.-79+49128T>C NP_001305770.1:n.-79+49128T>C
XM_005258229.4:c.-78-103051T>C XP_005258286.1:n.-78-103051T>C
XM_011525861.2:c.-187+49128T>C XP_011524163.1:n.-187+49128T>C
XM_011525863.3:c.-179+49128T>C XP_011524165.1:n.-179+49128T>C
XM_011525864.2:c.-179+49128T>C XP_011524166.1:n.-179+49128T>C
XM_011525865.3:c.-175+49128T>C XP_011524167.1:n.-175+49128T>C
XM_011525869.3:c.-187+49128T>C XP_011524171.1:n.-187+49128T>C
XM_011525870.2:c.-78-103051T>C XP_011524172.1:n.-78-103051T>C
XM_017025605.1:c.-187+49128T>C XP_016881094.1:n.-187+49128T>C
XM_017025606.2:c.-311+49128T>C XP_016881095.1:n.-311+49128T>C
XM_017025607.1:c.-311+49128T>C XP_016881096.1:n.-311+49128T>C
XM_017025608.1:c.-187+49128T>C XP_016881097.1:n.-187+49128T>C
XM_017025609.2:c.-79+49128T>C XP_016881098.1:n.-79+49128T>C
NM_001318841.2:c.-79+49128T>C MANE Select NP_001305770.1:n.-79+49128T>C
NM_001371284.1:c.-334+49128T>C NP_001358213.1:n.-334+49128T>C
NM_001371285.1:c.-255-103051T>C NP_001358214.1:n.-255-103051T>C
NM_001371286.1:c.-78-103051T>C NP_001358215.1:n.-78-103051T>C
NM_001371287.1:c.-211+49128T>C NP_001358216.1:n.-211+49128T>C
NM_001371290.1:c.-343-36748T>C NP_001358219.1:n.-343-36748T>C
NM_001371291.1:c.-208+49128T>C NP_001358220.1:n.-208+49128T>C
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