Canonical Allele Identifier: CA2128944756
Gene: NFKBIA HGNC NCBI

Linked Data

dbSNP Id: rs2052773319

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.35404721G>A , CM000676.2:g.35404721G>A GRCh38
NC_000014.8:g.35873927G>A , CM000676.1:g.35873927G>A GRCh37
NC_000014.7:g.34943678G>A NCBI36
NG_007571.1:g.5018C>T , LRG_89:g.5018C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000553342.2:c.-77C>T ENSP00000451281.2:n.-77C>T
ENST00000557459.2:n.22C>T
ENST00000697957.1:n.29C>T
ENST00000697958.1:n.22C>T
ENST00000697959.1:n.29C>T
ENST00000697960.1:n.9C>T
ENST00000697961.1:c.-77C>T ENSP00000513487.1:n.-77C>T
ENST00000216797.10:c.-77C>T MANE Select ENSP00000216797.6:n.-77C>T
ENST00000216797.9:c.-77C>T ENSP00000216797.5:n.-77C>T
ENST00000555629.1:n.29C>T
ENST00000557140.5:c.-77C>T ENSP00000451257.1:n.-77C>T
ENST00000557459.1:n.22C>T
NM_020529.2:c.-77C>T , LRG_89t1:c.-77C>T NP_065390.1:n.-77C>T
NM_020529.3:c.-77C>T MANE Select NP_065390.1:n.-77C>T