Canonical Allele Identifier: CA258863232

Gene: NFKBIA

Linked Data

• dbSNP Id: rs368072323
• gnomAD v3: 14-35404706-C-G
• gnomAD v4: 14-35404706-C-G
• MyVariant Identifiers: chr14:g.35873912C>G (hg19) ; chr14:g.35404706C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35404706C>G , CM000676.2:g.35404706C>G	GRCh38
NC_000014.8:g.35873912C>G , CM000676.1:g.35873912C>G	GRCh37
NC_000014.7:g.34943663C>G	NCBI36
NG_007571.1:g.5033G>C , LRG_89:g.5033G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553342.2:c.-62G>C	ENSP00000451281.2:n.-62G>C
ENST00000557459.2:n.37G>C
ENST00000697957.1:n.44G>C
ENST00000697958.1:n.37G>C
ENST00000697959.1:n.44G>C
ENST00000697960.1:n.24G>C
ENST00000697961.1:c.-62G>C	ENSP00000513487.1:n.-62G>C
ENST00000216797.10:c.-62G>C MANE Select	ENSP00000216797.6:n.-62G>C
ENST00000216797.9:c.-62G>C	ENSP00000216797.5:n.-62G>C
ENST00000554001.5:c.-62G>C	ENSP00000450537.1:n.-62G>C
ENST00000555629.1:n.44G>C
ENST00000557140.5:c.-62G>C	ENSP00000451257.1:n.-62G>C
ENST00000557459.1:n.37G>C
NM_020529.2:c.-62G>C , LRG_89t1:c.-62G>C	NP_065390.1:n.-62G>C
NM_020529.3:c.-62G>C MANE Select	NP_065390.1:n.-62G>C