Canonical Allele Identifier: CA4802945
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 411786
dbSNP Id: rs151070415
gnomAD v2: 8-90990485-C-T
gnomAD v3: 8-89978257-C-T
gnomAD v4: 8-89978257-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89978257C>T , CM000670.2:g.89978257C>T GRCh38
NC_000008.10:g.90990485C>T , CM000670.1:g.90990485C>T GRCh37
NC_000008.9:g.91059661C>T NCBI36
NG_008860.1:g.11415G>A , LRG_158:g.11415G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.1849G>A
ENST00000517337.2:c.301G>A ENSP00000429971.2:p.Ala101Thr
ENST00000523444.2:c.301G>A ENSP00000428252.2:p.Ala101Thr
ENST00000697292.1:c.547G>A ENSP00000513229.1:p.Ala183Thr
ENST00000697293.1:c.547G>A ENSP00000513230.1:p.Ala183Thr
ENST00000697294.1:c.*158G>A ENSP00000513231.1:n.*158G>A
ENST00000697295.1:c.37+6268G>A ENSP00000513232.1:n.37+6268G>A
ENST00000697296.1:c.*215G>A ENSP00000513233.1:n.*215G>A
ENST00000697297.1:n.2332G>A
ENST00000697298.1:c.301G>A ENSP00000513234.1:p.Ala101Thr
ENST00000697299.1:c.301G>A ENSP00000513235.1:p.Ala101Thr
ENST00000697300.1:c.*151G>A ENSP00000513236.1:n.*151G>A
ENST00000697301.1:c.*68G>A ENSP00000513237.1:n.*68G>A
ENST00000697302.1:c.*68G>A ENSP00000513238.1:n.*68G>A
ENST00000697303.1:c.*151G>A ENSP00000513239.1:n.*151G>A
ENST00000697304.1:c.547G>A ENSP00000513240.1:p.Ala183Thr
ENST00000697306.1:c.480+2477G>A ENSP00000513241.1:n.480+2477G>A
ENST00000697307.1:c.547G>A ENSP00000513242.1:p.Ala183Thr
ENST00000697308.1:c.547G>A ENSP00000513243.1:p.Ala183Thr
ENST00000697309.1:c.547G>A ENSP00000513244.1:p.Ala183Thr
ENST00000697310.1:c.547G>A ENSP00000513245.1:p.Ala183Thr
ENST00000697311.1:c.547G>A ENSP00000513246.1:p.Ala183Thr
ENST00000697312.1:c.480+2477G>A ENSP00000513247.1:n.480+2477G>A
ENST00000697313.1:n.2338G>A
ENST00000697314.1:n.2338G>A
ENST00000697315.1:c.547G>A ENSP00000513248.1:p.Ala183Thr
ENST00000697316.1:n.668G>A
ENST00000697317.1:n.657G>A
ENST00000697318.1:n.659G>A
ENST00000265433.8:c.547G>A MANE Select ENSP00000265433.4:p.Ala183Thr
ENST00000265433.7:c.547G>A ENSP00000265433.3:p.Ala183Thr
ENST00000396252.6:c.*420G>A ENSP00000379551.2:n.*420G>A
ENST00000409330.5:c.301G>A ENSP00000386924.1:p.Ala101Thr
ENST00000517772.5:c.301G>A ENSP00000428717.1:p.Ala101Thr
ENST00000519426.5:c.320+3118G>A ENSP00000430983.1:n.320+3118G>A
NM_001024688.2:c.301G>A NP_001019859.1:p.Ala101Thr
NM_002485.4:c.547G>A , LRG_158t1:c.547G>A NP_002476.2:p.Ala183Thr
XM_011517044.1:c.523G>A XP_011515346.1:p.Ala175Thr
XM_011517045.1:c.301G>A XP_011515347.1:p.Ala101Thr
XM_011517046.1:c.547G>A XP_011515348.1:p.Ala183Thr
XR_928335.1:n.684G>A
XM_017013460.1:c.-333G>A XP_016868949.1:n.-333G>A
XM_017013462.2:c.-296+2477G>A XP_016868951.1:n.-296+2477G>A
XM_024447163.1:c.301G>A XP_024302931.1:p.Ala101Thr
XM_024447164.1:c.301G>A XP_024302932.1:p.Ala101Thr
XM_024447165.1:c.-333G>A XP_024302933.1:n.-333G>A
NM_002485.5:c.547G>A MANE Select NP_002476.2:p.Ala183Thr
NM_001024688.3:c.301G>A NP_001019859.1:p.Ala101Thr