Canonical Allele Identifier: CA371663426

Gene: NBN

Linked Data

• ClinVar Variation Id: 837991
• ClinVar RCV Id: RCV001039445 ; RCV003478669
• dbSNP Id: rs755171159
• gnomAD v4: 8-89982813-C-T
• MyVariant Identifiers: chr8:g.90995041C>T (hg19) ; chr8:g.89982813C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89982813C>T , CM000670.2:g.89982813C>T	GRCh38
NC_000008.10:g.90995041C>T , CM000670.1:g.90995041C>T	GRCh37
NC_000008.9:g.91064217C>T	NCBI36
NG_008860.1:g.6859G>A , LRG_158:g.6859G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.184G>A
ENST00000517337.2:c.-217G>A	ENSP00000429971.2:n.-217G>A
ENST00000523444.2:c.-217G>A	ENSP00000428252.2:n.-217G>A
ENST00000697292.1:c.80G>A	ENSP00000513229.1:p.Gly27Glu
ENST00000697293.1:c.80G>A	ENSP00000513230.1:p.Gly27Glu
ENST00000697294.1:c.80G>A	ENSP00000513231.1:p.Gly27Glu
ENST00000697295.1:c.37+1712G>A	ENSP00000513232.1:n.37+1712G>A
ENST00000697296.1:c.80G>A	ENSP00000513233.1:p.Gly27Glu
ENST00000697297.1:n.186G>A
ENST00000697298.1:c.-217G>A	ENSP00000513234.1:n.-217G>A
ENST00000697299.1:c.-75-1290G>A	ENSP00000513235.1:n.-75-1290G>A
ENST00000697300.1:c.-217G>A	ENSP00000513236.1:n.-217G>A
ENST00000697301.1:c.-217G>A	ENSP00000513237.1:n.-217G>A
ENST00000697302.1:c.80G>A	ENSP00000513238.1:p.Gly27Glu
ENST00000697303.1:c.80G>A	ENSP00000513239.1:p.Gly27Glu
ENST00000697304.1:c.80G>A	ENSP00000513240.1:p.Gly27Glu
ENST00000697306.1:c.80G>A	ENSP00000513241.1:p.Gly27Glu
ENST00000697307.1:c.80G>A	ENSP00000513242.1:p.Gly27Glu
ENST00000697308.1:c.80G>A	ENSP00000513243.1:p.Gly27Glu
ENST00000697309.1:c.80G>A	ENSP00000513244.1:p.Gly27Glu
ENST00000697310.1:c.80G>A	ENSP00000513245.1:p.Gly27Glu
ENST00000697311.1:c.80G>A	ENSP00000513246.1:p.Gly27Glu
ENST00000697312.1:c.80G>A	ENSP00000513247.1:p.Gly27Glu
ENST00000697313.1:n.192G>A
ENST00000697314.1:n.192G>A
ENST00000697315.1:c.80G>A	ENSP00000513248.1:p.Gly27Glu
ENST00000697316.1:n.201G>A
ENST00000697317.1:n.190G>A
ENST00000697318.1:n.192G>A
ENST00000265433.8:c.80G>A MANE Select	ENSP00000265433.4:p.Gly27Glu
ENST00000265433.7:c.80G>A	ENSP00000265433.3:p.Gly27Glu
ENST00000396252.6:c.80G>A	ENSP00000379551.2:p.Gly27Glu
ENST00000409330.5:c.-167G>A	ENSP00000386924.1:n.-167G>A
ENST00000494804.1:n.184G>A
ENST00000517337.1:c.-217G>A	ENSP00000429971.1:n.-217G>A
ENST00000519426.5:c.80G>A	ENSP00000430983.1:p.Gly27Glu
ENST00000523444.1:c.80G>A	ENSP00000428252.1:p.Gly27Glu
NM_001024688.2:c.-217G>A	NP_001019859.1:n.-217G>A
NM_002485.4:c.80G>A , LRG_158t1:c.80G>A	NP_002476.2:p.Gly27Glu
XM_011517044.1:c.56G>A	XP_011515346.1:p.Gly19Glu
XM_011517045.1:c.-217G>A	XP_011515347.1:n.-217G>A
XM_011517046.1:c.80G>A	XP_011515348.1:p.Gly27Glu
XR_928335.1:n.217G>A
XM_017013460.1:c.-940G>A	XP_016868949.1:n.-940G>A
XM_017013462.2:c.-746G>A	XP_016868951.1:n.-746G>A
XM_024447163.1:c.-167G>A	XP_024302931.1:n.-167G>A
XM_024447165.1:c.-890G>A	XP_024302933.1:n.-890G>A
NM_002485.5:c.80G>A MANE Select	NP_002476.2:p.Gly27Glu
NM_001024688.3:c.-217G>A	NP_001019859.1:n.-217G>A