Canonical Allele Identifier: CA485909114

Gene: NFKBIA

Linked Data

• dbSNP Id: rs1229016752
• gnomAD v2: 14-35873830-G-A
• gnomAD v4: 14-35404624-G-A
• MyVariant Identifiers: chr14:g.35873830G>A (hg19) ; chr14:g.35404624G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35404624G>A , CM000676.2:g.35404624G>A	GRCh38
NC_000014.8:g.35873830G>A , CM000676.1:g.35873830G>A	GRCh37
NC_000014.7:g.34943581G>A	NCBI36
NG_007571.1:g.5115C>T , LRG_89:g.5115C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000553342.2:c.21C>T	ENSP00000451281.2:p.Arg7=
ENST00000557459.2:n.119C>T
ENST00000697957.1:n.126C>T
ENST00000697958.1:n.119C>T
ENST00000697959.1:n.126C>T
ENST00000697960.1:n.106C>T
ENST00000697961.1:c.21C>T	ENSP00000513487.1:p.Arg7=
ENST00000697966.1:n.49-10C>T
ENST00000216797.10:c.21C>T MANE Select	ENSP00000216797.6:p.Arg7=
ENST00000216797.9:c.21C>T	ENSP00000216797.5:p.Arg7=
ENST00000553342.1:c.21C>T	ENSP00000451281.1:p.Arg7=
ENST00000554001.5:c.21C>T	ENSP00000450537.1:p.Arg7=
ENST00000555629.1:n.126C>T
ENST00000557100.5:n.77C>T
ENST00000557140.5:c.21C>T	ENSP00000451257.1:p.Arg7=
ENST00000557459.1:n.119C>T
NM_020529.2:c.21C>T , LRG_89t1:c.21C>T	NP_065390.1:p.Arg7=
NM_020529.3:c.21C>T MANE Select	NP_065390.1:p.Arg7=