Canonical Allele Identifier: CA371676462

Gene: NBN

Linked Data

• ClinVar Variation Id: 939438
• ClinVar RCV Id: RCV001208843
• dbSNP Id: rs876658336
• MyVariant Identifiers: chr8:g.90958435G>C (hg19) ; chr8:g.89946207G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89946207G>C , CM000670.2:g.89946207G>C	GRCh38
NC_000008.10:g.90958435G>C , CM000670.1:g.90958435G>C	GRCh37
NC_000008.9:g.91027611G>C	NCBI36
NG_008860.1:g.43465C>G , LRG_158:g.43465C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.3305C>G
ENST00000517337.2:c.1757C>G	ENSP00000429971.2:p.Thr586Ser
ENST00000523444.2:c.1757C>G	ENSP00000428252.2:p.Thr586Ser
ENST00000697292.1:c.2003C>G	ENSP00000513229.1:p.Thr668Ser
ENST00000697293.1:c.2003C>G	ENSP00000513230.1:p.Thr668Ser
ENST00000697294.1:c.*1614C>G	ENSP00000513231.1:n.*1614C>G
ENST00000697295.1:c.*1312C>G	ENSP00000513232.1:n.*1312C>G
ENST00000697296.1:c.*1671C>G	ENSP00000513233.1:n.*1671C>G
ENST00000697297.1:n.3788C>G
ENST00000697298.1:c.1757C>G	ENSP00000513234.1:p.Thr586Ser
ENST00000697299.1:c.1757C>G	ENSP00000513235.1:p.Thr586Ser
ENST00000697300.1:c.*1607C>G	ENSP00000513236.1:n.*1607C>G
ENST00000697301.1:c.*1524C>G	ENSP00000513237.1:n.*1524C>G
ENST00000697302.1:c.*1524C>G	ENSP00000513238.1:n.*1524C>G
ENST00000697303.1:c.*1607C>G	ENSP00000513239.1:n.*1607C>G
ENST00000697304.1:c.1691C>G	ENSP00000513240.1:p.Thr564Ser
ENST00000697306.1:c.*2554C>G	ENSP00000513241.1:n.*2554C>G
ENST00000697307.1:c.1846-2841C>G	ENSP00000513242.1:n.1846-2841C>G
ENST00000697308.1:c.1934C>G	ENSP00000513243.1:p.Thr645Ser
ENST00000697309.1:c.2003C>G	ENSP00000513244.1:p.Thr668Ser
ENST00000697310.1:c.2003C>G	ENSP00000513245.1:p.Thr668Ser
ENST00000697311.1:c.2003C>G	ENSP00000513246.1:p.Thr668Ser
ENST00000697312.1:c.*1401C>G	ENSP00000513247.1:n.*1401C>G
ENST00000697313.1:n.2688-10595C>G
ENST00000697314.1:n.3636+7037C>G
ENST00000697315.1:c.2003C>G	ENSP00000513248.1:p.Thr668Ser
ENST00000697316.1:n.2124C>G
ENST00000697317.1:n.2094C>G
ENST00000265433.8:c.2003C>G MANE Select	ENSP00000265433.4:p.Thr668Ser
ENST00000265433.7:c.2003C>G	ENSP00000265433.3:p.Thr668Ser
ENST00000396252.6:c.*1876C>G	ENSP00000379551.2:n.*1876C>G
ENST00000409330.5:c.1757C>G	ENSP00000386924.1:p.Thr586Ser
ENST00000520325.1:n.419C>G
ENST00000613033.1:c.180+1617C>G	ENSP00000484487.1:n.180+1617C>G
NM_001024688.2:c.1757C>G	NP_001019859.1:p.Thr586Ser
NM_002485.4:c.2003C>G , LRG_158t1:c.2003C>G	NP_002476.2:p.Thr668Ser
XM_011517044.1:c.1979C>G	XP_011515346.1:p.Thr660Ser
XM_011517045.1:c.1757C>G	XP_011515347.1:p.Thr586Ser
XM_017013460.1:c.1124C>G	XP_016868949.1:p.Thr375Ser
XM_017013462.2:c.1124C>G	XP_016868951.1:p.Thr375Ser
XM_024447163.1:c.1757C>G	XP_024302931.1:p.Thr586Ser
XM_024447164.1:c.1757C>G	XP_024302932.1:p.Thr586Ser
XM_024447165.1:c.1124C>G	XP_024302933.1:p.Thr375Ser
NM_002485.5:c.2003C>G MANE Select	NP_002476.2:p.Thr668Ser
NM_001024688.3:c.1757C>G	NP_001019859.1:p.Thr586Ser