Canonical Allele Identifier: CA371662913

Gene: NBN

Linked Data

• ClinVar Variation Id: 1008920
• ClinVar RCV Id: RCV001306333
• dbSNP Id: rs769700749
• MyVariant Identifiers: chr8:g.90994960A>G (hg19) ; chr8:g.89982732A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89982732A>G , CM000670.2:g.89982732A>G	GRCh38
NC_000008.10:g.90994960A>G , CM000670.1:g.90994960A>G	GRCh37
NC_000008.9:g.91064136A>G	NCBI36
NG_008860.1:g.6940T>C , LRG_158:g.6940T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000494804.2:n.265T>C
ENST00000517337.2:c.-136T>C	ENSP00000429971.2:n.-136T>C
ENST00000523444.2:c.-136T>C	ENSP00000428252.2:n.-136T>C
ENST00000697292.1:c.161T>C	ENSP00000513229.1:p.Val54Ala
ENST00000697293.1:c.161T>C	ENSP00000513230.1:p.Val54Ala
ENST00000697294.1:c.161T>C	ENSP00000513231.1:p.Val54Ala
ENST00000697295.1:c.37+1793T>C	ENSP00000513232.1:n.37+1793T>C
ENST00000697296.1:c.161T>C	ENSP00000513233.1:p.Val54Ala
ENST00000697297.1:n.267T>C
ENST00000697298.1:c.-136T>C	ENSP00000513234.1:n.-136T>C
ENST00000697299.1:c.-75-1209T>C	ENSP00000513235.1:n.-75-1209T>C
ENST00000697300.1:c.-136T>C	ENSP00000513236.1:n.-136T>C
ENST00000697301.1:c.-136T>C	ENSP00000513237.1:n.-136T>C
ENST00000697302.1:c.161T>C	ENSP00000513238.1:p.Val54Ala
ENST00000697303.1:c.161T>C	ENSP00000513239.1:p.Val54Ala
ENST00000697304.1:c.161T>C	ENSP00000513240.1:p.Val54Ala
ENST00000697306.1:c.161T>C	ENSP00000513241.1:p.Val54Ala
ENST00000697307.1:c.161T>C	ENSP00000513242.1:p.Val54Ala
ENST00000697308.1:c.161T>C	ENSP00000513243.1:p.Val54Ala
ENST00000697309.1:c.161T>C	ENSP00000513244.1:p.Val54Ala
ENST00000697310.1:c.161T>C	ENSP00000513245.1:p.Val54Ala
ENST00000697311.1:c.161T>C	ENSP00000513246.1:p.Val54Ala
ENST00000697312.1:c.161T>C	ENSP00000513247.1:p.Val54Ala
ENST00000697313.1:n.273T>C
ENST00000697314.1:n.273T>C
ENST00000697315.1:c.161T>C	ENSP00000513248.1:p.Val54Ala
ENST00000697316.1:n.282T>C
ENST00000697317.1:n.271T>C
ENST00000697318.1:n.273T>C
ENST00000265433.8:c.161T>C MANE Select	ENSP00000265433.4:p.Val54Ala
ENST00000265433.7:c.161T>C	ENSP00000265433.3:p.Val54Ala
ENST00000396252.6:c.161T>C	ENSP00000379551.2:p.Val54Ala
ENST00000409330.5:c.-86T>C	ENSP00000386924.1:n.-86T>C
ENST00000494804.1:n.265T>C
ENST00000517337.1:c.-136T>C	ENSP00000429971.1:n.-136T>C
ENST00000519426.5:c.161T>C	ENSP00000430983.1:p.Val54Ala
ENST00000523444.1:c.161T>C	ENSP00000428252.1:p.Val54Ala
NM_001024688.2:c.-136T>C	NP_001019859.1:n.-136T>C
NM_002485.4:c.161T>C , LRG_158t1:c.161T>C	NP_002476.2:p.Val54Ala
XM_011517044.1:c.137T>C	XP_011515346.1:p.Val46Ala
XM_011517045.1:c.-136T>C	XP_011515347.1:n.-136T>C
XM_011517046.1:c.161T>C	XP_011515348.1:p.Val54Ala
XR_928335.1:n.298T>C
XM_017013460.1:c.-859T>C	XP_016868949.1:n.-859T>C
XM_017013462.2:c.-665T>C	XP_016868951.1:n.-665T>C
XM_024447163.1:c.-86T>C	XP_024302931.1:n.-86T>C
XM_024447165.1:c.-809T>C	XP_024302933.1:n.-809T>C
NM_002485.5:c.161T>C MANE Select	NP_002476.2:p.Val54Ala
NM_001024688.3:c.-136T>C	NP_001019859.1:n.-136T>C