Canonical Allele Identifier: CA258863265

Gene: NFKBIA

Linked Data

• dbSNP Id: rs1012166920
• gnomAD v3: 14-35404719-T-C
• gnomAD v4: 14-35404719-T-C
• MyVariant Identifiers: chr14:g.35873925T>C (hg19) ; chr14:g.35404719T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35404719T>C , CM000676.2:g.35404719T>C	GRCh38
NC_000014.8:g.35873925T>C , CM000676.1:g.35873925T>C	GRCh37
NC_000014.7:g.34943676T>C	NCBI36
NG_007571.1:g.5020A>G , LRG_89:g.5020A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553342.2:c.-75A>G	ENSP00000451281.2:n.-75A>G
ENST00000557459.2:n.24A>G
ENST00000697957.1:n.31A>G
ENST00000697958.1:n.24A>G
ENST00000697959.1:n.31A>G
ENST00000697960.1:n.11A>G
ENST00000697961.1:c.-75A>G	ENSP00000513487.1:n.-75A>G
ENST00000216797.10:c.-75A>G MANE Select	ENSP00000216797.6:n.-75A>G
ENST00000216797.9:c.-75A>G	ENSP00000216797.5:n.-75A>G
ENST00000555629.1:n.31A>G
ENST00000557140.5:c.-75A>G	ENSP00000451257.1:n.-75A>G
ENST00000557459.1:n.24A>G
NM_020529.2:c.-75A>G , LRG_89t1:c.-75A>G	NP_065390.1:n.-75A>G
NM_020529.3:c.-75A>G MANE Select	NP_065390.1:n.-75A>G