Canonical Allele Identifier: CA2128942791
Gene: NFKBIA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.35401527T= , CM000676.2:g.35401527T= GRCh38
NC_000014.8:g.35870733T= , CM000676.1:g.35870733T= GRCh37
NC_000014.7:g.34940484T= NCBI36
NG_007571.1:g.8212A= , LRG_89:g.8212A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553342.2:c.*486A= ENSP00000451281.2:n.*486A=
ENST00000697954.1:n.1649A=
ENST00000697955.1:n.1688A=
ENST00000697956.1:n.1716A=
ENST00000697957.1:n.1835A=
ENST00000216797.10:c.*486A= MANE Select ENSP00000216797.6:n.*486A=
ENST00000216797.9:c.*486A= ENSP00000216797.5:n.*486A=
NM_020529.2:c.*486A= , LRG_89t1:c.*486A= NP_065390.1:n.*486A=
NM_020529.3:c.*486A= MANE Select NP_065390.1:n.*486A=
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