Canonical Allele Identifier: CA15550766
Gene: IKBKB HGNC NCBI

Linked Data

dbSNP Id: rs12676482
gnomAD v2: 8-42174077-G-A
gnomAD v3: 8-42316559-G-A
gnomAD v4: 8-42316559-G-A
MyVariant Identifiers: chr8:g.42174077G>A (hg19) chr8:g.42316559G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42316559G>A , CM000670.2:g.42316559G>A GRCh38
NC_000008.10:g.42174077G>A , CM000670.1:g.42174077G>A GRCh37
NC_000008.9:g.42293234G>A NCBI36
NG_041793.1:g.50258G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000416505.7:c.594-151G>A
ENST00000520810.6:c.931-151G>A MANE Select ENSP00000430684.1:n.931-151G>A
ENST00000520835.7:c.739-151G>A ENSP00000430868.2:n.739-151G>A
ENST00000629753.2:c.*745-151G>A ENSP00000486961.2:n.*745-151G>A
ENST00000648136.2:n.695-151G>A
ENST00000649612.3:c.695-151G>A
ENST00000676525.1:c.533-151G>A ENSP00000503997.1:n.533-151G>A
ENST00000342222.6:c.*492-151G>A ENSP00000339151.2:n.*492-151G>A
ENST00000416505.5:c.754-151G>A ENSP00000404920.2:n.754-151G>A
ENST00000517890.5:c.*689-151G>A ENSP00000428799.1:n.*689-151G>A
ENST00000517917.5:n.817-151G>A
ENST00000518647.5:n.1029-151G>A
ENST00000518679.5:c.*212-151G>A ENSP00000430557.1:n.*212-151G>A
ENST00000520201.5:n.935-151G>A
ENST00000520655.5:c.931-151G>A ENSP00000428922.1:n.931-151G>A
ENST00000520810.5:c.931-151G>A ENSP00000430684.1:n.931-151G>A
ENST00000520835.5:c.925-151G>A ENSP00000430868.1:n.925-151G>A
ENST00000521661.5:c.931-151G>A ENSP00000428186.1:n.931-151G>A
ENST00000522147.4:c.106-14648G>A ENSP00000428892.1:n.106-14648G>A
ENST00000523105.5:c.*689-151G>A ENSP00000429239.1:n.*689-151G>A
ENST00000523517.5:c.931-151G>A ENSP00000430114.1:n.931-151G>A
ENST00000629753.1:c.931-151G>A ENSP00000486961.1:n.931-151G>A
NM_001190720.2:c.925-151G>A NP_001177649.1:n.925-151G>A
NM_001242778.1:c.754-151G>A NP_001229707.1:n.754-151G>A
NM_001556.2:c.931-151G>A NP_001547.1:n.931-151G>A
NR_033818.1:n.1173-151G>A
NR_033819.1:n.1117-151G>A
NR_040009.1:n.1117-151G>A
XM_005273490.1:c.931-151G>A XP_005273547.1:n.931-151G>A
XM_005273491.3:c.754-151G>A XP_005273548.1:n.754-151G>A
XM_005273492.2:c.931-151G>A XP_005273549.1:n.931-151G>A
XM_005273493.2:c.616-151G>A XP_005273550.1:n.616-151G>A
XM_005273494.1:c.931-151G>A XP_005273551.1:n.931-151G>A
XM_005273495.1:c.301-151G>A XP_005273552.1:n.301-151G>A
XM_005273496.2:c.301-151G>A XP_005273553.1:n.301-151G>A
XM_005273498.2:c.301-151G>A XP_005273555.1:n.301-151G>A
XM_011544517.1:c.931-151G>A XP_011542819.1:n.931-151G>A
XM_011544518.1:c.781-151G>A XP_011542820.1:n.781-151G>A
XM_011544519.1:c.754-151G>A XP_011542821.1:n.754-151G>A
XM_011544520.1:c.676-151G>A XP_011542822.1:n.676-151G>A
XM_011544521.1:c.301-151G>A XP_011542823.1:n.301-151G>A
XM_011544522.1:c.94-151G>A XP_011542824.1:n.94-151G>A
XR_949402.1:n.1017-151G>A
NM_001556.3:c.931-151G>A MANE Select NP_001547.1:n.931-151G>A
XM_005273490.3:c.931-151G>A XP_005273547.1:n.931-151G>A
XM_005273491.5:c.754-151G>A XP_005273548.1:n.754-151G>A
XM_005273492.4:c.931-151G>A XP_005273549.1:n.931-151G>A
XM_005273493.4:c.616-151G>A XP_005273550.1:n.616-151G>A
XM_005273494.3:c.931-151G>A XP_005273551.1:n.931-151G>A
XM_005273495.2:c.301-151G>A XP_005273552.1:n.301-151G>A
XM_005273496.4:c.301-151G>A XP_005273553.1:n.301-151G>A
XM_005273498.4:c.301-151G>A XP_005273555.1:n.301-151G>A
XM_011544517.2:c.931-151G>A XP_011542819.1:n.931-151G>A
XM_011544518.2:c.781-151G>A XP_011542820.1:n.781-151G>A
XM_011544519.2:c.754-151G>A XP_011542821.1:n.754-151G>A
XM_011544520.2:c.676-151G>A XP_011542822.1:n.676-151G>A
XM_011544521.2:c.301-151G>A XP_011542823.1:n.301-151G>A
XM_011544522.2:c.94-151G>A XP_011542824.1:n.94-151G>A
XM_017013396.1:c.94-151G>A XP_016868885.1:n.94-151G>A
XR_001745530.2:n.1115-151G>A
XR_949402.3:n.1597-151G>A
NM_001242778.2:c.754-151G>A NP_001229707.1:n.754-151G>A
NR_033818.2:n.1173-151G>A
NR_033819.2:n.1117-151G>A
NR_040009.2:n.1117-151G>A
NM_001190720.3:c.739-151G>A NP_001177649.2:n.739-151G>A
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