Canonical Allele Identifier: CA1801415511

Gene: NBN

Linked Data

• dbSNP Id: rs1809734466
• gnomAD v4: 8-89937237-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89937237T>C , CM000670.2:g.89937237T>C	GRCh38
NC_000008.10:g.90949465T>C , CM000670.1:g.90949465T>C	GRCh37
NC_000008.9:g.91018641T>C	NCBI36
NG_008860.1:g.52435A>G , LRG_158:g.52435A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474821.2:n.3443A>G
ENST00000494804.2:n.3487-162A>G
ENST00000517337.2:c.1939-162A>G	ENSP00000429971.2:n.1939-162A>G
ENST00000523444.2:c.1939-162A>G	ENSP00000428252.2:n.1939-162A>G
ENST00000697292.1:c.2185-162A>G	ENSP00000513229.1:n.2185-162A>G
ENST00000697293.1:c.2236-162A>G	ENSP00000513230.1:n.2236-162A>G
ENST00000697294.1:c.*1796-162A>G	ENSP00000513231.1:n.*1796-162A>G
ENST00000697295.1:c.*1494-162A>G	ENSP00000513232.1:n.*1494-162A>G
ENST00000697296.1:c.*1853-162A>G	ENSP00000513233.1:n.*1853-162A>G
ENST00000697297.1:n.3970-162A>G
ENST00000697298.1:c.1939-162A>G	ENSP00000513234.1:n.1939-162A>G
ENST00000697299.1:c.1939-162A>G	ENSP00000513235.1:n.1939-162A>G
ENST00000697300.1:c.*1789-162A>G	ENSP00000513236.1:n.*1789-162A>G
ENST00000697301.1:c.*1706-162A>G	ENSP00000513237.1:n.*1706-162A>G
ENST00000697302.1:c.*1706-162A>G	ENSP00000513238.1:n.*1706-162A>G
ENST00000697303.1:c.*1789-162A>G	ENSP00000513239.1:n.*1789-162A>G
ENST00000697304.1:c.1873-162A>G	ENSP00000513240.1:n.1873-162A>G
ENST00000697305.1:n.2452-162A>G
ENST00000697306.1:c.*2736-162A>G	ENSP00000513241.1:n.*2736-162A>G
ENST00000697307.1:c.1960-162A>G	ENSP00000513242.1:n.1960-162A>G
ENST00000697308.1:c.2116-162A>G	ENSP00000513243.1:n.2116-162A>G
ENST00000697309.1:c.2185-1625A>G	ENSP00000513244.1:n.2185-1625A>G
ENST00000697310.1:c.2185-162A>G	ENSP00000513245.1:n.2185-162A>G
ENST00000697311.1:c.*450-162A>G	ENSP00000513246.1:n.*450-162A>G
ENST00000697312.1:c.*1638-162A>G	ENSP00000513247.1:n.*1638-162A>G
ENST00000697313.1:n.2688-1625A>G
ENST00000697314.1:n.3637-1625A>G
ENST00000697315.1:c.*89-162A>G	ENSP00000513248.1:n.*89-162A>G
ENST00000697316.1:n.2306-162A>G
ENST00000265433.8:c.2185-162A>G MANE Select	ENSP00000265433.4:n.2185-162A>G
ENST00000265433.7:c.2185-162A>G	ENSP00000265433.3:n.2185-162A>G
ENST00000396252.6:c.*2058-162A>G	ENSP00000379551.2:n.*2058-162A>G
ENST00000409330.5:c.1939-162A>G	ENSP00000386924.1:n.1939-162A>G
ENST00000474821.1:n.111A>G
ENST00000613033.1:c.295-162A>G	ENSP00000484487.1:n.295-162A>G
NM_001024688.2:c.1939-162A>G	NP_001019859.1:n.1939-162A>G
NM_002485.4:c.2185-162A>G , LRG_158t1:c.2185-162A>G	NP_002476.2:n.2185-162A>G
XM_011517044.1:c.2161-162A>G	XP_011515346.1:n.2161-162A>G
XM_011517045.1:c.1939-162A>G	XP_011515347.1:n.1939-162A>G
XM_017013460.1:c.1306-162A>G	XP_016868949.1:n.1306-162A>G
XM_017013462.2:c.1306-162A>G	XP_016868951.1:n.1306-162A>G
XM_024447163.1:c.1939-162A>G	XP_024302931.1:n.1939-162A>G
XM_024447164.1:c.1939-162A>G	XP_024302932.1:n.1939-162A>G
XM_024447165.1:c.1306-162A>G	XP_024302933.1:n.1306-162A>G
NM_002485.5:c.2185-162A>G MANE Select	NP_002476.2:n.2185-162A>G
NM_001024688.3:c.1939-162A>G	NP_001019859.1:n.1939-162A>G