Canonical Allele Identifier: CA389455347
Gene: NFKBIA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.35404560G>C , CM000676.2:g.35404560G>C GRCh38
NC_000014.8:g.35873766G>C , CM000676.1:g.35873766G>C GRCh37
NC_000014.7:g.34943517G>C NCBI36
NG_007571.1:g.5179C>G , LRG_89:g.5179C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000553342.2:c.85C>G ENSP00000451281.2:p.Arg29Gly
ENST00000557459.2:n.183C>G
ENST00000697957.1:n.190C>G
ENST00000697958.1:n.183C>G
ENST00000697959.1:n.190C>G
ENST00000697960.1:n.170C>G
ENST00000697961.1:c.85C>G ENSP00000513487.1:p.Arg29Gly
ENST00000697966.1:n.103C>G
ENST00000216797.10:c.85C>G MANE Select ENSP00000216797.6:p.Arg29Gly
ENST00000216797.9:c.85C>G ENSP00000216797.5:p.Arg29Gly
ENST00000553342.1:c.85C>G ENSP00000451281.1:p.Arg29Gly
ENST00000554001.5:c.85C>G ENSP00000450537.1:p.Arg29Gly
ENST00000555629.1:n.190C>G
ENST00000557100.5:n.141C>G
ENST00000557140.5:c.85C>G ENSP00000451257.1:p.Arg29Gly
ENST00000557459.1:n.183C>G
NM_020529.2:c.85C>G , LRG_89t1:c.85C>G NP_065390.1:p.Arg29Gly
NM_020529.3:c.85C>G MANE Select NP_065390.1:p.Arg29Gly