Canonical Allele Identifier: CA645181824

Gene: IKBKG

Linked Data

• dbSNP Id: rs1557236843
• gnomAD v2: X-153792487-C-T
• MyVariant Identifiers: chrX:g.153792487C>T (hg19) ; chrX:g.154564272C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154564272C>T , CM000685.2:g.154564272C>T	GRCh38
NC_000023.10:g.153792487C>T , CM000685.1:g.153792487C>T	GRCh37
NC_000023.9:g.153445681C>T	NCBI36
NG_009896.1:g.27029C>T , LRG_70:g.27029C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413620.6:c.1082-47C>T	ENSP00000398579.2:n.1082-47C>T
ENST00000422680.6:c.1118-47C>T	ENSP00000390368.3:n.1118-47C>T
ENST00000440286.6:c.1118-47C>T	ENSP00000394934.2:n.1118-47C>T
ENST00000445622.6:c.1118-47C>T	ENSP00000395205.2:n.1118-47C>T
ENST00000615186.5:c.716-47C>T	ENSP00000479144.2:n.716-47C>T
ENST00000689906.1:c.965-47C>T	ENSP00000508630.1:n.965-47C>T
ENST00000692948.1:c.1175-47C>T	ENSP00000508773.1:n.1175-47C>T
ENST00000594239.6:c.1118-47C>T MANE Select	ENSP00000471166.1:n.1118-47C>T
ENST00000594239.5:c.1118-47C>T	ENSP00000471166.1:n.1118-47C>T
ENST00000611071.4:c.1118-47C>T	ENSP00000479662.1:n.1118-47C>T
ENST00000611176.4:c.821-47C>T	ENSP00000478616.1:n.821-47C>T
ENST00000612051.1:c.*1110-47C>T	ENSP00000480431.1:n.*1110-47C>T
ENST00000615874.4:c.1094-47C>T	ENSP00000483381.1:n.1094-47C>T
ENST00000617207.4:c.1115-47C>T	ENSP00000484023.1:n.1115-47C>T
ENST00000618670.4:c.1322-47C>T	ENSP00000483825.1:n.1322-47C>T
ENST00000619941.4:c.1097-47C>T	ENSP00000478979.1:n.1097-47C>T
NM_001099856.3:c.1322-47C>T	NP_001093326.2:n.1322-47C>T
NM_001099857.2:c.1118-47C>T	NP_001093327.1:n.1118-47C>T
NM_001145255.2:c.821-47C>T	NP_001138727.1:n.821-47C>T
NM_003639.4:c.1118-47C>T	NP_003630.1:n.1118-47C>T
XM_005274760.3:c.1319-47C>T	XP_005274817.1:n.1319-47C>T
XM_005274761.3:c.1321+252C>T	XP_005274818.1:n.1321+252C>T
XM_005274764.3:c.1115-47C>T	XP_005274821.1:n.1115-47C>T
XM_011531203.1:c.1169-47C>T	XP_011529505.1:n.1169-47C>T
XM_011531204.1:c.1118-47C>T	XP_011529506.1:n.1118-47C>T
XM_011531205.1:c.1118-47C>T	XP_011529507.1:n.1118-47C>T
NM_001099856.4:c.1322-47C>T	NP_001093326.2:n.1322-47C>T
NM_001321396.1:c.1118-47C>T	NP_001308325.1:n.1118-47C>T
NM_001321397.1:c.1115-47C>T	NP_001308326.1:n.1115-47C>T
NM_001099856.6:c.1322-47C>T	NP_001093326.2:n.1322-47C>T
NM_001099857.4:c.1118-47C>T	NP_001093327.1:n.1118-47C>T
NM_001145255.4:c.821-47C>T	NP_001138727.1:n.821-47C>T
NM_001321396.3:c.1118-47C>T	NP_001308325.1:n.1118-47C>T
NM_001321397.3:c.1115-47C>T	NP_001308326.1:n.1115-47C>T
NM_001377312.1:c.1118-47C>T	NP_001364241.1:n.1118-47C>T
NM_001377313.1:c.1115-47C>T	NP_001364242.1:n.1115-47C>T
NM_001377314.1:c.962-47C>T	NP_001364243.1:n.962-47C>T
NM_001377315.1:c.749-47C>T	NP_001364244.1:n.749-47C>T
NR_165197.1:n.987-47C>T
NM_001099857.5:c.1118-47C>T MANE Select	NP_001093327.1:n.1118-47C>T