Canonical Allele Identifier: CA705268066

Gene: NFKBIA

Linked Data

• dbSNP Id: rs1170593961
• gnomAD v4: 14-35401662-G-C
• MyVariant Identifiers: chr14:g.35870868G>C (hg19) ; chr14:g.35401662G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35401662G>C , CM000676.2:g.35401662G>C	GRCh38
NC_000014.8:g.35870868G>C , CM000676.1:g.35870868G>C	GRCh37
NC_000014.7:g.34940619G>C	NCBI36
NG_007571.1:g.8077C>G , LRG_89:g.8077C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553342.2:c.*351C>G	ENSP00000451281.2:n.*351C>G
ENST00000697954.1:n.1514C>G
ENST00000697955.1:n.1553C>G
ENST00000697956.1:n.1581C>G
ENST00000697957.1:n.1700C>G
ENST00000697958.1:n.2355C>G
ENST00000697959.1:n.2033C>G
ENST00000697960.1:n.2449C>G
ENST00000697961.1:c.*720C>G	ENSP00000513487.1:n.*720C>G
ENST00000216797.10:c.*351C>G MANE Select	ENSP00000216797.6:n.*351C>G
ENST00000216797.9:c.*351C>G	ENSP00000216797.5:n.*351C>G
ENST00000554001.5:c.*947C>G	ENSP00000450537.1:n.*947C>G
ENST00000557140.5:c.*351C>G	ENSP00000451257.1:n.*351C>G
ENST00000557389.1:c.*351C>G	ENSP00000450514.1:n.*351C>G
NM_020529.2:c.*351C>G , LRG_89t1:c.*351C>G	NP_065390.1:n.*351C>G
NM_020529.3:c.*351C>G MANE Select	NP_065390.1:n.*351C>G