Canonical Allele Identifier: CA2335257631

Gene: NFKBIB

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38906009C>G , CM000681.2:g.38906009C>G	GRCh38
NC_000019.9:g.39396649C>G , CM000681.1:g.39396649C>G	GRCh37
NC_000019.8:g.44088489C>G	NCBI36
NG_029624.1:g.11310C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313582.6:c.619+474C>G MANE Select	ENSP00000312988.5:n.619+474C>G
ENST00000313582.5:c.619+474C>G	ENSP00000312988.5:n.619+474C>G
ENST00000392079.7:c.361+474C>G	ENSP00000375929.4:n.361+474C>G
ENST00000509705.3:c.*365+474C>G	ENSP00000438598.2:n.*365+474C>G
ENST00000572515.5:c.619+474C>G	ENSP00000459728.1:n.619+474C>G
ENST00000575359.5:c.391+474C>G	ENSP00000458685.1:n.391+474C>G
ENST00000576510.5:c.361+474C>G	ENSP00000461617.1:n.361+474C>G
NM_001243116.1:c.361+474C>G	NP_001230045.1:n.361+474C>G
NM_002503.4:c.619+474C>G	NP_002494.2:n.619+474C>G
NR_040515.1:n.666+474C>G
XM_006723226.2:c.523+474C>G	XP_006723289.2:n.523+474C>G
XM_006723227.2:c.361+474C>G	XP_006723290.2:n.361+474C>G
XM_006723227.3:c.604+474C>G	XP_006723290.3:n.604+474C>G
NM_002503.5:c.619+474C>G MANE Select	NP_002494.2:n.619+474C>G
NM_001369699.1:c.619+474C>G	NP_001356628.1:n.619+474C>G
NM_001369700.1:c.343+474C>G	NP_001356629.1:n.343+474C>G
NR_040515.2:n.627+474C>G
NR_161470.1:n.514+474C>G
NM_001243116.2:c.361+474C>G	NP_001230045.1:n.361+474C>G