Canonical Allele Identifier: CA371660055

Gene: NBN

Linked Data

• ClinVar Variation Id: 2808926
• ClinVar RCV Id: RCV003618364
• gnomAD v4: 8-89978219-C-A
• MyVariant Identifiers: chr8:g.90990447C>A (hg19) ; chr8:g.89978219C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89978219C>A , CM000670.2:g.89978219C>A	GRCh38
NC_000008.10:g.90990447C>A , CM000670.1:g.90990447C>A	GRCh37
NC_000008.9:g.91059623C>A	NCBI36
NG_008860.1:g.11453G>T , LRG_158:g.11453G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.1886+1G>T
ENST00000517337.2:c.338+1G>T	ENSP00000429971.2:n.338+1G>T
ENST00000523444.2:c.338+1G>T	ENSP00000428252.2:n.338+1G>T
ENST00000697292.1:c.584+1G>T	ENSP00000513229.1:n.584+1G>T
ENST00000697293.1:c.584+1G>T	ENSP00000513230.1:n.584+1G>T
ENST00000697294.1:c.*195+1G>T	ENSP00000513231.1:n.*195+1G>T
ENST00000697295.1:c.37+6306G>T	ENSP00000513232.1:n.37+6306G>T
ENST00000697296.1:c.*252+1G>T	ENSP00000513233.1:n.*252+1G>T
ENST00000697297.1:n.2369+1G>T
ENST00000697298.1:c.338+1G>T	ENSP00000513234.1:n.338+1G>T
ENST00000697299.1:c.338+1G>T	ENSP00000513235.1:n.338+1G>T
ENST00000697300.1:c.*188+1G>T	ENSP00000513236.1:n.*188+1G>T
ENST00000697301.1:c.*105+1G>T	ENSP00000513237.1:n.*105+1G>T
ENST00000697302.1:c.*105+1G>T	ENSP00000513238.1:n.*105+1G>T
ENST00000697303.1:c.*188+1G>T	ENSP00000513239.1:n.*188+1G>T
ENST00000697304.1:c.584+1G>T	ENSP00000513240.1:n.584+1G>T
ENST00000697306.1:c.480+2515G>T	ENSP00000513241.1:n.480+2515G>T
ENST00000697307.1:c.584+1G>T	ENSP00000513242.1:n.584+1G>T
ENST00000697308.1:c.584+1G>T	ENSP00000513243.1:n.584+1G>T
ENST00000697309.1:c.584+1G>T	ENSP00000513244.1:n.584+1G>T
ENST00000697310.1:c.584+1G>T	ENSP00000513245.1:n.584+1G>T
ENST00000697311.1:c.584+1G>T	ENSP00000513246.1:n.584+1G>T
ENST00000697312.1:c.480+2515G>T	ENSP00000513247.1:n.480+2515G>T
ENST00000697313.1:n.2375+1G>T
ENST00000697314.1:n.2375+1G>T
ENST00000697315.1:c.584+1G>T	ENSP00000513248.1:n.584+1G>T
ENST00000697316.1:n.705+1G>T
ENST00000697317.1:n.694+1G>T
ENST00000697318.1:n.696+1G>T
ENST00000265433.8:c.584+1G>T MANE Select	ENSP00000265433.4:n.584+1G>T
ENST00000265433.7:c.584+1G>T	ENSP00000265433.3:n.584+1G>T
ENST00000396252.6:c.*457+1G>T	ENSP00000379551.2:n.*457+1G>T
ENST00000409330.5:c.338+1G>T	ENSP00000386924.1:n.338+1G>T
ENST00000517772.5:c.338+1G>T	ENSP00000428717.1:n.338+1G>T
ENST00000519426.5:c.320+3156G>T	ENSP00000430983.1:n.320+3156G>T
NM_001024688.2:c.338+1G>T	NP_001019859.1:n.338+1G>T
NM_002485.4:c.584+1G>T , LRG_158t1:c.584+1G>T	NP_002476.2:n.584+1G>T
XM_011517044.1:c.560+1G>T	XP_011515346.1:n.560+1G>T
XM_011517045.1:c.338+1G>T	XP_011515347.1:n.338+1G>T
XM_011517046.1:c.584+1G>T	XP_011515348.1:n.584+1G>T
XR_928335.1:n.721+1G>T
XM_017013460.1:c.-296+1G>T	XP_016868949.1:n.-296+1G>T
XM_017013462.2:c.-296+2515G>T	XP_016868951.1:n.-296+2515G>T
XM_024447163.1:c.338+1G>T	XP_024302931.1:n.338+1G>T
XM_024447164.1:c.338+1G>T	XP_024302932.1:n.338+1G>T
XM_024447165.1:c.-296+1G>T	XP_024302933.1:n.-296+1G>T
NM_002485.5:c.584+1G>T MANE Select	NP_002476.2:n.584+1G>T
NM_001024688.3:c.338+1G>T	NP_001019859.1:n.338+1G>T