Canonical Allele Identifier: CA705268518

Gene: NFKBIA

Linked Data

• dbSNP Id: rs898611454
• gnomAD v4: 14-35404680-C-T
• MyVariant Identifiers: chr14:g.35873886C>T (hg19) ; chr14:g.35404680C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35404680C>T , CM000676.2:g.35404680C>T	GRCh38
NC_000014.8:g.35873886C>T , CM000676.1:g.35873886C>T	GRCh37
NC_000014.7:g.34943637C>T	NCBI36
NG_007571.1:g.5059G>A , LRG_89:g.5059G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553342.2:c.-36G>A	ENSP00000451281.2:n.-36G>A
ENST00000557459.2:n.63G>A
ENST00000697957.1:n.70G>A
ENST00000697958.1:n.63G>A
ENST00000697959.1:n.70G>A
ENST00000697960.1:n.50G>A
ENST00000697961.1:c.-36G>A	ENSP00000513487.1:n.-36G>A
ENST00000697966.1:n.22G>A
ENST00000216797.10:c.-36G>A MANE Select	ENSP00000216797.6:n.-36G>A
ENST00000216797.9:c.-36G>A	ENSP00000216797.5:n.-36G>A
ENST00000554001.5:c.-36G>A	ENSP00000450537.1:n.-36G>A
ENST00000555629.1:n.70G>A
ENST00000557100.5:n.21G>A
ENST00000557140.5:c.-36G>A	ENSP00000451257.1:n.-36G>A
ENST00000557459.1:n.63G>A
NM_020529.2:c.-36G>A , LRG_89t1:c.-36G>A	NP_065390.1:n.-36G>A
NM_020529.3:c.-36G>A MANE Select	NP_065390.1:n.-36G>A