Canonical Allele Identifier: CA4802888
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1759967
dbSNP Id: rs754243946
gnomAD v2: 8-90982724-T-C
gnomAD v4: 8-89970496-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.89970496T>C , CM000670.2:g.89970496T>C GRCh38
NC_000008.10:g.90982724T>C , CM000670.1:g.90982724T>C GRCh37
NC_000008.9:g.91051900T>C NCBI36
NG_008860.1:g.19176A>G , LRG_158:g.19176A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000494804.2:n.2066A>G
ENST00000517337.2:c.518A>G ENSP00000429971.2:p.Glu173Gly
ENST00000523444.2:c.518A>G ENSP00000428252.2:p.Glu173Gly
ENST00000697292.1:c.764A>G ENSP00000513229.1:p.Glu255Gly
ENST00000697293.1:c.764A>G ENSP00000513230.1:p.Glu255Gly
ENST00000697294.1:c.*375A>G ENSP00000513231.1:n.*375A>G
ENST00000697295.1:c.*73A>G ENSP00000513232.1:n.*73A>G
ENST00000697296.1:c.*432A>G ENSP00000513233.1:n.*432A>G
ENST00000697297.1:n.2549A>G
ENST00000697298.1:c.518A>G ENSP00000513234.1:p.Glu173Gly
ENST00000697299.1:c.518A>G ENSP00000513235.1:p.Glu173Gly
ENST00000697300.1:c.*368A>G ENSP00000513236.1:n.*368A>G
ENST00000697301.1:c.*285A>G ENSP00000513237.1:n.*285A>G
ENST00000697302.1:c.*285A>G ENSP00000513238.1:n.*285A>G
ENST00000697303.1:c.*368A>G ENSP00000513239.1:n.*368A>G
ENST00000697304.1:c.585-5989A>G ENSP00000513240.1:n.585-5989A>G
ENST00000697306.1:c.480+10238A>G ENSP00000513241.1:n.480+10238A>G
ENST00000697307.1:c.764A>G ENSP00000513242.1:p.Glu255Gly
ENST00000697308.1:c.764A>G ENSP00000513243.1:p.Glu255Gly
ENST00000697309.1:c.764A>G ENSP00000513244.1:p.Glu255Gly
ENST00000697310.1:c.764A>G ENSP00000513245.1:p.Glu255Gly
ENST00000697311.1:c.764A>G ENSP00000513246.1:p.Glu255Gly
ENST00000697312.1:c.*162A>G ENSP00000513247.1:n.*162A>G
ENST00000697313.1:n.2555A>G
ENST00000697314.1:n.2555A>G
ENST00000697315.1:c.764A>G ENSP00000513248.1:p.Glu255Gly
ENST00000697316.1:n.885A>G
ENST00000697317.1:n.874A>G
ENST00000697318.1:n.876A>G
ENST00000265433.8:c.764A>G MANE Select ENSP00000265433.4:p.Glu255Gly
ENST00000265433.7:c.764A>G ENSP00000265433.3:p.Glu255Gly
ENST00000396252.6:c.*637A>G ENSP00000379551.2:n.*637A>G
ENST00000409330.5:c.518A>G ENSP00000386924.1:p.Glu173Gly
NM_001024688.2:c.518A>G NP_001019859.1:p.Glu173Gly
NM_002485.4:c.764A>G , LRG_158t1:c.764A>G NP_002476.2:p.Glu255Gly
XM_011517044.1:c.740A>G XP_011515346.1:p.Glu247Gly
XM_011517045.1:c.518A>G XP_011515347.1:p.Glu173Gly
XM_011517046.1:c.764A>G XP_011515348.1:p.Glu255Gly
XR_928335.1:n.901A>G
XM_017013460.1:c.-116A>G XP_016868949.1:n.-116A>G
XM_017013462.2:c.-116A>G XP_016868951.1:n.-116A>G
XM_024447163.1:c.518A>G XP_024302931.1:p.Glu173Gly
XM_024447164.1:c.518A>G XP_024302932.1:p.Glu173Gly
XM_024447165.1:c.-116A>G XP_024302933.1:n.-116A>G
NM_002485.5:c.764A>G MANE Select NP_002476.2:p.Glu255Gly
NM_001024688.3:c.518A>G NP_001019859.1:p.Glu173Gly