Canonical Allele Identifier: CA461831046

Gene: NBN

Linked Data

• ClinVar Variation Id: 1640121
• ClinVar RCV Id: RCV002131562
• dbSNP Id: rs1335414652
• gnomAD v2: 8-90983464-T-G
• gnomAD v4: 8-89971236-T-G
• MyVariant Identifiers: chr8:g.90983464T>G (hg19) ; chr8:g.89971236T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89971236T>G , CM000670.2:g.89971236T>G	GRCh38
NC_000008.10:g.90983464T>G , CM000670.1:g.90983464T>G	GRCh37
NC_000008.9:g.91052640T>G	NCBI36
NG_008860.1:g.18436A>C , LRG_158:g.18436A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000494804.2:n.1941A>C
ENST00000517337.2:c.393A>C	ENSP00000429971.2:p.Ser131=
ENST00000523444.2:c.393A>C	ENSP00000428252.2:p.Ser131=
ENST00000697292.1:c.639A>C	ENSP00000513229.1:p.Ser213=
ENST00000697293.1:c.639A>C	ENSP00000513230.1:p.Ser213=
ENST00000697294.1:c.*250A>C	ENSP00000513231.1:n.*250A>C
ENST00000697295.1:c.92A>C	ENSP00000513232.1:p.Gln31Pro
ENST00000697296.1:c.*307A>C	ENSP00000513233.1:n.*307A>C
ENST00000697297.1:n.2424A>C
ENST00000697298.1:c.393A>C	ENSP00000513234.1:p.Ser131=
ENST00000697299.1:c.393A>C	ENSP00000513235.1:p.Ser131=
ENST00000697300.1:c.*243A>C	ENSP00000513236.1:n.*243A>C
ENST00000697301.1:c.*160A>C	ENSP00000513237.1:n.*160A>C
ENST00000697302.1:c.*160A>C	ENSP00000513238.1:n.*160A>C
ENST00000697303.1:c.*243A>C	ENSP00000513239.1:n.*243A>C
ENST00000697304.1:c.585-6729A>C	ENSP00000513240.1:n.585-6729A>C
ENST00000697306.1:c.480+9498A>C	ENSP00000513241.1:n.480+9498A>C
ENST00000697307.1:c.639A>C	ENSP00000513242.1:p.Ser213=
ENST00000697308.1:c.639A>C	ENSP00000513243.1:p.Ser213=
ENST00000697309.1:c.639A>C	ENSP00000513244.1:p.Ser213=
ENST00000697310.1:c.639A>C	ENSP00000513245.1:p.Ser213=
ENST00000697311.1:c.639A>C	ENSP00000513246.1:p.Ser213=
ENST00000697312.1:c.*37A>C	ENSP00000513247.1:n.*37A>C
ENST00000697313.1:n.2430A>C
ENST00000697314.1:n.2430A>C
ENST00000697315.1:c.639A>C	ENSP00000513248.1:p.Ser213=
ENST00000697316.1:n.760A>C
ENST00000697317.1:n.749A>C
ENST00000697318.1:n.751A>C
ENST00000265433.8:c.639A>C MANE Select	ENSP00000265433.4:p.Ser213=
ENST00000265433.7:c.639A>C	ENSP00000265433.3:p.Ser213=
ENST00000396252.6:c.*512A>C	ENSP00000379551.2:n.*512A>C
ENST00000409330.5:c.393A>C	ENSP00000386924.1:p.Ser131=
ENST00000517772.5:c.393A>C	ENSP00000428717.1:p.Ser131=
ENST00000519426.5:c.375A>C	ENSP00000430983.1:p.Ser125=
NM_001024688.2:c.393A>C	NP_001019859.1:p.Ser131=
NM_002485.4:c.639A>C , LRG_158t1:c.639A>C	NP_002476.2:p.Ser213=
XM_011517044.1:c.615A>C	XP_011515346.1:p.Ser205=
XM_011517045.1:c.393A>C	XP_011515347.1:p.Ser131=
XM_011517046.1:c.639A>C	XP_011515348.1:p.Ser213=
XR_928335.1:n.776A>C
XM_017013460.1:c.-241A>C	XP_016868949.1:n.-241A>C
XM_017013462.2:c.-241A>C	XP_016868951.1:n.-241A>C
XM_024447163.1:c.393A>C	XP_024302931.1:p.Ser131=
XM_024447164.1:c.393A>C	XP_024302932.1:p.Ser131=
XM_024447165.1:c.-241A>C	XP_024302933.1:n.-241A>C
NM_002485.5:c.639A>C MANE Select	NP_002476.2:p.Ser213=
NM_001024688.3:c.393A>C	NP_001019859.1:p.Ser131=