Canonical Allele Identifier: CA2717735772

Gene: NBN

Linked Data

• dbSNP Id: rs764356392

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89984522T>A , CM000670.2:g.89984522T>A	GRCh38
NC_000008.10:g.90996750T>A , CM000670.1:g.90996750T>A	GRCh37
NC_000008.9:g.91065926T>A	NCBI36
NG_008860.1:g.5150A>T , LRG_158:g.5150A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.141+3A>T
ENST00000523444.2:c.-260+3A>T	ENSP00000428252.2:n.-260+3A>T
ENST00000697292.1:c.37+3A>T	ENSP00000513229.1:n.37+3A>T
ENST00000697293.1:c.37+3A>T	ENSP00000513230.1:n.37+3A>T
ENST00000697294.1:c.37+3A>T	ENSP00000513231.1:n.37+3A>T
ENST00000697295.1:c.37+3A>T	ENSP00000513232.1:n.37+3A>T
ENST00000697296.1:c.37+3A>T	ENSP00000513233.1:n.37+3A>T
ENST00000697297.1:n.143+3A>T
ENST00000697298.1:c.-443+3A>T	ENSP00000513234.1:n.-443+3A>T
ENST00000697299.1:c.-76+3A>T	ENSP00000513235.1:n.-76+3A>T
ENST00000697300.1:c.-260+3A>T	ENSP00000513236.1:n.-260+3A>T
ENST00000697301.1:c.-260+3A>T	ENSP00000513237.1:n.-260+3A>T
ENST00000697302.1:c.37+3A>T	ENSP00000513238.1:n.37+3A>T
ENST00000697303.1:c.37+3A>T	ENSP00000513239.1:n.37+3A>T
ENST00000697304.1:c.37+3A>T	ENSP00000513240.1:n.37+3A>T
ENST00000697306.1:c.37+3A>T	ENSP00000513241.1:n.37+3A>T
ENST00000697307.1:c.37+3A>T	ENSP00000513242.1:n.37+3A>T
ENST00000697308.1:c.37+3A>T	ENSP00000513243.1:n.37+3A>T
ENST00000697309.1:c.37+3A>T	ENSP00000513244.1:n.37+3A>T
ENST00000697310.1:c.37+3A>T	ENSP00000513245.1:n.37+3A>T
ENST00000697311.1:c.37+3A>T	ENSP00000513246.1:n.37+3A>T
ENST00000697312.1:c.37+3A>T	ENSP00000513247.1:n.37+3A>T
ENST00000697313.1:n.149+3A>T
ENST00000697314.1:n.149+3A>T
ENST00000697315.1:c.37+3A>T	ENSP00000513248.1:n.37+3A>T
ENST00000697316.1:n.158+3A>T
ENST00000697317.1:n.147+3A>T
ENST00000697318.1:n.149+3A>T
ENST00000265433.8:c.37+3A>T MANE Select	ENSP00000265433.4:n.37+3A>T
ENST00000265433.7:c.37+3A>T	ENSP00000265433.3:n.37+3A>T
ENST00000396252.6:c.37+3A>T	ENSP00000379551.2:n.37+3A>T
ENST00000494804.1:n.141+3A>T
ENST00000519426.5:c.37+3A>T	ENSP00000430983.1:n.37+3A>T
ENST00000523444.1:c.37+3A>T	ENSP00000428252.1:n.37+3A>T
NM_001024688.2:c.-260+3A>T	NP_001019859.1:n.-260+3A>T
NM_002485.4:c.37+3A>T , LRG_158t1:c.37+3A>T	NP_002476.2:n.37+3A>T
XM_011517046.1:c.37+3A>T	XP_011515348.1:n.37+3A>T
XR_928335.1:n.174+3A>T
XM_017013460.1:c.-983+3A>T	XP_016868949.1:n.-983+3A>T
XM_017013462.2:c.-789+3A>T	XP_016868951.1:n.-789+3A>T
XM_024447165.1:c.-933+3A>T	XP_024302933.1:n.-933+3A>T
NM_002485.5:c.37+3A>T MANE Select	NP_002476.2:n.37+3A>T
NM_001024688.3:c.-260+3A>T	NP_001019859.1:n.-260+3A>T