Canonical Allele Identifier: CA705267979

Gene: NFKBIA

Linked Data

• dbSNP Id: rs1296279185
• gnomAD v4: 14-35401527-T-C
• MyVariant Identifiers: chr14:g.35870733T>C (hg19) ; chr14:g.35401527T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.35401527T>C , CM000676.2:g.35401527T>C	GRCh38
NC_000014.8:g.35870733T>C , CM000676.1:g.35870733T>C	GRCh37
NC_000014.7:g.34940484T>C	NCBI36
NG_007571.1:g.8212A>G , LRG_89:g.8212A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553342.2:c.*486A>G	ENSP00000451281.2:n.*486A>G
ENST00000697954.1:n.1649A>G
ENST00000697955.1:n.1688A>G
ENST00000697956.1:n.1716A>G
ENST00000697957.1:n.1835A>G
ENST00000216797.10:c.*486A>G MANE Select	ENSP00000216797.6:n.*486A>G
ENST00000216797.9:c.*486A>G	ENSP00000216797.5:n.*486A>G
NM_020529.2:c.*486A>G , LRG_89t1:c.*486A>G	NP_065390.1:n.*486A>G
NM_020529.3:c.*486A>G MANE Select	NP_065390.1:n.*486A>G