Canonical Allele Identifier: CA7155606

Gene: NFKBIA

Linked Data

• ClinVar Variation Id: 2155610
• ClinVar RCV Id: RCV003083922
• dbSNP Id: rs748171915
• ExAC: 14:35873824 C / T
• gnomAD v2: 14-35873824-C-T
• gnomAD v3: 14-35404618-C-T
• gnomAD v4: 14-35404618-C-T
• MyVariant Identifiers: chr14:g.35873824C>T (hg19) ; chr14:g.35404618C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35404618C>T , CM000676.2:g.35404618C>T	GRCh38
NC_000014.8:g.35873824C>T , CM000676.1:g.35873824C>T	GRCh37
NC_000014.7:g.34943575C>T	NCBI36
NG_007571.1:g.5121G>A , LRG_89:g.5121G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000553342.2:c.27G>A	ENSP00000451281.2:p.Gln9=
ENST00000557459.2:n.125G>A
ENST00000697957.1:n.132G>A
ENST00000697958.1:n.125G>A
ENST00000697959.1:n.132G>A
ENST00000697960.1:n.112G>A
ENST00000697961.1:c.27G>A	ENSP00000513487.1:p.Gln9=
ENST00000697966.1:n.49-4G>A
ENST00000216797.10:c.27G>A MANE Select	ENSP00000216797.6:p.Gln9=
ENST00000216797.9:c.27G>A	ENSP00000216797.5:p.Gln9=
ENST00000553342.1:c.27G>A	ENSP00000451281.1:p.Gln9=
ENST00000554001.5:c.27G>A	ENSP00000450537.1:p.Gln9=
ENST00000555629.1:n.132G>A
ENST00000557100.5:n.83G>A
ENST00000557140.5:c.27G>A	ENSP00000451257.1:p.Gln9=
ENST00000557459.1:n.125G>A
NM_020529.2:c.27G>A , LRG_89t1:c.27G>A	NP_065390.1:p.Gln9=
NM_020529.3:c.27G>A MANE Select	NP_065390.1:p.Gln9=