Canonical Allele Identifier: CA2624569314

Gene: NFKBIA

Linked Data

• dbSNP Id: rs540282095
• gnomAD v4: 14-35404685-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35404685C>A , CM000676.2:g.35404685C>A	GRCh38
NC_000014.8:g.35873891C>A , CM000676.1:g.35873891C>A	GRCh37
NC_000014.7:g.34943642C>A	NCBI36
NG_007571.1:g.5054G>T , LRG_89:g.5054G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553342.2:c.-41G>T	ENSP00000451281.2:n.-41G>T
ENST00000557459.2:n.58G>T
ENST00000697957.1:n.65G>T
ENST00000697958.1:n.58G>T
ENST00000697959.1:n.65G>T
ENST00000697960.1:n.45G>T
ENST00000697961.1:c.-41G>T	ENSP00000513487.1:n.-41G>T
ENST00000697966.1:n.17G>T
ENST00000216797.10:c.-41G>T MANE Select	ENSP00000216797.6:n.-41G>T
ENST00000216797.9:c.-41G>T	ENSP00000216797.5:n.-41G>T
ENST00000554001.5:c.-41G>T	ENSP00000450537.1:n.-41G>T
ENST00000555629.1:n.65G>T
ENST00000557100.5:n.16G>T
ENST00000557140.5:c.-41G>T	ENSP00000451257.1:n.-41G>T
ENST00000557459.1:n.58G>T
NM_020529.2:c.-41G>T , LRG_89t1:c.-41G>T	NP_065390.1:n.-41G>T
NM_020529.3:c.-41G>T MANE Select	NP_065390.1:n.-41G>T