Canonical Allele Identifier: CA2466732610

Gene: IKBKG

Linked Data

• dbSNP Id: rs2071052058
• gnomAD v4: X-154556014-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154556014A>G , CM000685.2:g.154556014A>G	GRCh38
NC_000023.10:g.153784229A>G , CM000685.1:g.153784229A>G	GRCh37
NC_000023.9:g.153437423A>G	NCBI36
NG_009896.1:g.18771A>G , LRG_70:g.18771A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000413620.6:c.152-151A>G	ENSP00000398579.2:n.152-151A>G
ENST00000422680.6:c.188-151A>G	ENSP00000390368.3:n.188-151A>G
ENST00000440286.6:c.188-151A>G	ENSP00000394934.2:n.188-151A>G
ENST00000445622.6:c.188-151A>G	ENSP00000395205.2:n.188-151A>G
ENST00000492469.3:c.188-151A>G	ENSP00000484275.2:n.188-151A>G
ENST00000615186.5:c.-87-279A>G	ENSP00000479144.2:n.-87-279A>G
ENST00000686378.1:c.188-151A>G	ENSP00000509444.1:n.188-151A>G
ENST00000686774.1:c.188-151A>G	ENSP00000510218.1:n.188-151A>G
ENST00000687445.1:n.563-151A>G
ENST00000689906.1:c.188-151A>G	ENSP00000508630.1:n.188-151A>G
ENST00000692816.1:n.563-151A>G
ENST00000692948.1:c.188-151A>G	ENSP00000508773.1:n.188-151A>G
ENST00000693029.1:n.563-151A>G
ENST00000594239.6:c.188-151A>G MANE Select	ENSP00000471166.1:n.188-151A>G
ENST00000413620.5:c.152-151A>G	ENSP00000398579.1:n.152-151A>G
ENST00000422680.5:c.188-151A>G	ENSP00000390368.2:n.188-151A>G
ENST00000440286.5:c.188-151A>G	ENSP00000394934.1:n.188-151A>G
ENST00000445622.5:c.188-151A>G	ENSP00000395205.1:n.188-151A>G
ENST00000492469.2:c.20-151A>G	ENSP00000484275.1:n.20-151A>G
ENST00000594239.5:c.188-151A>G	ENSP00000471166.1:n.188-151A>G
ENST00000611071.4:c.188-151A>G	ENSP00000479662.1:n.188-151A>G
ENST00000611176.4:c.188-151A>G	ENSP00000478616.1:n.188-151A>G
ENST00000612051.1:c.*180-151A>G	ENSP00000480431.1:n.*180-151A>G
ENST00000615186.4:c.-87-279A>G	ENSP00000479144.1:n.-87-279A>G
ENST00000615874.4:c.188-151A>G	ENSP00000483381.1:n.188-151A>G
ENST00000617207.4:c.188-151A>G	ENSP00000484023.1:n.188-151A>G
ENST00000617838.1:n.199+3825A>G
ENST00000618670.4:c.392-151A>G	ENSP00000483825.1:n.392-151A>G
ENST00000619941.4:c.188-151A>G	ENSP00000478979.1:n.188-151A>G
NM_001099856.3:c.392-151A>G	NP_001093326.2:n.392-151A>G
NM_001099857.2:c.188-151A>G	NP_001093327.1:n.188-151A>G
NM_001145255.2:c.188-151A>G	NP_001138727.1:n.188-151A>G
NM_003639.4:c.188-151A>G	NP_003630.1:n.188-151A>G
XM_005274760.3:c.392-151A>G	XP_005274817.1:n.392-151A>G
XM_005274761.3:c.392-151A>G	XP_005274818.1:n.392-151A>G
XM_005274764.3:c.188-151A>G	XP_005274821.1:n.188-151A>G
XM_011531203.1:c.392-151A>G	XP_011529505.1:n.392-151A>G
XM_011531204.1:c.188-151A>G	XP_011529506.1:n.188-151A>G
XM_011531205.1:c.188-151A>G	XP_011529507.1:n.188-151A>G
XM_011531206.1:c.392-151A>G	XP_011529508.1:n.392-151A>G
XM_011531207.1:c.392-151A>G	XP_011529509.1:n.392-151A>G
NM_001099856.4:c.392-151A>G	NP_001093326.2:n.392-151A>G
NM_001321396.1:c.188-151A>G	NP_001308325.1:n.188-151A>G
NM_001321397.1:c.188-151A>G	NP_001308326.1:n.188-151A>G
NM_001099856.6:c.392-151A>G	NP_001093326.2:n.392-151A>G
NM_001099857.4:c.188-151A>G	NP_001093327.1:n.188-151A>G
NM_001145255.4:c.188-151A>G	NP_001138727.1:n.188-151A>G
NM_001321396.3:c.188-151A>G	NP_001308325.1:n.188-151A>G
NM_001321397.3:c.188-151A>G	NP_001308326.1:n.188-151A>G
NM_001377312.1:c.188-151A>G	NP_001364241.1:n.188-151A>G
NM_001377313.1:c.188-151A>G	NP_001364242.1:n.188-151A>G
NM_001377314.1:c.188-151A>G	NP_001364243.1:n.188-151A>G
NM_001377315.1:c.188-151A>G	NP_001364244.1:n.188-151A>G
NR_165197.1:n.329-151A>G
NM_001099857.5:c.188-151A>G MANE Select	NP_001093327.1:n.188-151A>G