Canonical Allele Identifier: CA2128942818

Gene: NFKBIA

Linked Data

• dbSNP Id: rs2052726100

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35401584A>G , CM000676.2:g.35401584A>G	GRCh38
NC_000014.8:g.35870790A>G , CM000676.1:g.35870790A>G	GRCh37
NC_000014.7:g.34940541A>G	NCBI36
NG_007571.1:g.8155T>C , LRG_89:g.8155T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553342.2:c.*429T>C	ENSP00000451281.2:n.*429T>C
ENST00000697954.1:n.1592T>C
ENST00000697955.1:n.1631T>C
ENST00000697956.1:n.1659T>C
ENST00000697957.1:n.1778T>C
ENST00000697958.1:n.2433T>C
ENST00000697959.1:n.2111T>C
ENST00000697960.1:n.2527T>C
ENST00000697961.1:c.*798T>C	ENSP00000513487.1:n.*798T>C
ENST00000216797.10:c.*429T>C MANE Select	ENSP00000216797.6:n.*429T>C
ENST00000216797.9:c.*429T>C	ENSP00000216797.5:n.*429T>C
ENST00000554001.5:c.*1025T>C	ENSP00000450537.1:n.*1025T>C
ENST00000557140.5:c.*429T>C	ENSP00000451257.1:n.*429T>C
ENST00000557389.1:c.*429T>C	ENSP00000450514.1:n.*429T>C
NM_020529.2:c.*429T>C , LRG_89t1:c.*429T>C	NP_065390.1:n.*429T>C
NM_020529.3:c.*429T>C MANE Select	NP_065390.1:n.*429T>C