Canonical Allele Identifier: CA2128944707

Gene: NFKBIA

Linked Data

• dbSNP Id: rs919828562

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35404671G>C , CM000676.2:g.35404671G>C	GRCh38
NC_000014.8:g.35873877G>C , CM000676.1:g.35873877G>C	GRCh37
NC_000014.7:g.34943628G>C	NCBI36
NG_007571.1:g.5068C>G , LRG_89:g.5068C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553342.2:c.-27C>G	ENSP00000451281.2:n.-27C>G
ENST00000557459.2:n.72C>G
ENST00000697957.1:n.79C>G
ENST00000697958.1:n.72C>G
ENST00000697959.1:n.79C>G
ENST00000697960.1:n.59C>G
ENST00000697961.1:c.-27C>G	ENSP00000513487.1:n.-27C>G
ENST00000697966.1:n.31C>G
ENST00000216797.10:c.-27C>G MANE Select	ENSP00000216797.6:n.-27C>G
ENST00000216797.9:c.-27C>G	ENSP00000216797.5:n.-27C>G
ENST00000554001.5:c.-27C>G	ENSP00000450537.1:n.-27C>G
ENST00000555629.1:n.79C>G
ENST00000557100.5:n.30C>G
ENST00000557140.5:c.-27C>G	ENSP00000451257.1:n.-27C>G
ENST00000557459.1:n.72C>G
NM_020529.2:c.-27C>G , LRG_89t1:c.-27C>G	NP_065390.1:n.-27C>G
NM_020529.3:c.-27C>G MANE Select	NP_065390.1:n.-27C>G