Canonical Allele Identifier: CA349023

Gene: NBN

Linked Data

• ClinVar Variation Id: 219546
• ClinVar RCV Id: RCV000204839 ; RCV000220088 ; RCV000505926
• dbSNP Id: rs200564603
• ExAC: 8:90958400 C / T
• gnomAD v2: 8-90958400-C-T
• gnomAD v3: 8-89946172-C-T
• gnomAD v4: 8-89946172-C-T
• MyVariant Identifiers: chr8:g.90958400C>T (hg19) ; chr8:g.89946172C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89946172C>T , CM000670.2:g.89946172C>T	GRCh38
NC_000008.10:g.90958400C>T , CM000670.1:g.90958400C>T	GRCh37
NC_000008.9:g.91027576C>T	NCBI36
NG_008860.1:g.43500G>A , LRG_158:g.43500G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494804.2:n.3340G>A
ENST00000517337.2:c.1792G>A	ENSP00000429971.2:p.Gly598Ser
ENST00000523444.2:c.1792G>A	ENSP00000428252.2:p.Gly598Ser
ENST00000697292.1:c.2038G>A	ENSP00000513229.1:p.Gly680Ser
ENST00000697293.1:c.2038G>A	ENSP00000513230.1:p.Gly680Ser
ENST00000697294.1:c.*1649G>A	ENSP00000513231.1:n.*1649G>A
ENST00000697295.1:c.*1347G>A	ENSP00000513232.1:n.*1347G>A
ENST00000697296.1:c.*1706G>A	ENSP00000513233.1:n.*1706G>A
ENST00000697297.1:n.3823G>A
ENST00000697298.1:c.1792G>A	ENSP00000513234.1:p.Gly598Ser
ENST00000697299.1:c.1792G>A	ENSP00000513235.1:p.Gly598Ser
ENST00000697300.1:c.*1642G>A	ENSP00000513236.1:n.*1642G>A
ENST00000697301.1:c.*1559G>A	ENSP00000513237.1:n.*1559G>A
ENST00000697302.1:c.*1559G>A	ENSP00000513238.1:n.*1559G>A
ENST00000697303.1:c.*1642G>A	ENSP00000513239.1:n.*1642G>A
ENST00000697304.1:c.1726G>A	ENSP00000513240.1:p.Gly576Ser
ENST00000697306.1:c.*2589G>A	ENSP00000513241.1:n.*2589G>A
ENST00000697307.1:c.1846-2806G>A	ENSP00000513242.1:n.1846-2806G>A
ENST00000697308.1:c.1969G>A	ENSP00000513243.1:p.Gly657Ser
ENST00000697309.1:c.2038G>A	ENSP00000513244.1:p.Gly680Ser
ENST00000697310.1:c.2038G>A	ENSP00000513245.1:p.Gly680Ser
ENST00000697311.1:c.2038G>A	ENSP00000513246.1:p.Gly680Ser
ENST00000697312.1:c.*1436G>A	ENSP00000513247.1:n.*1436G>A
ENST00000697313.1:n.2688-10560G>A
ENST00000697314.1:n.3636+7072G>A
ENST00000697315.1:c.2038G>A	ENSP00000513248.1:p.Gly680Ser
ENST00000697316.1:n.2159G>A
ENST00000697317.1:n.2129G>A
ENST00000265433.8:c.2038G>A MANE Select	ENSP00000265433.4:p.Gly680Ser
ENST00000265433.7:c.2038G>A	ENSP00000265433.3:p.Gly680Ser
ENST00000396252.6:c.*1911G>A	ENSP00000379551.2:n.*1911G>A
ENST00000409330.5:c.1792G>A	ENSP00000386924.1:p.Gly598Ser
ENST00000520325.1:n.454G>A
ENST00000613033.1:c.180+1652G>A	ENSP00000484487.1:n.180+1652G>A
NM_001024688.2:c.1792G>A	NP_001019859.1:p.Gly598Ser
NM_002485.4:c.2038G>A , LRG_158t1:c.2038G>A	NP_002476.2:p.Gly680Ser
XM_011517044.1:c.2014G>A	XP_011515346.1:p.Gly672Ser
XM_011517045.1:c.1792G>A	XP_011515347.1:p.Gly598Ser
XM_017013460.1:c.1159G>A	XP_016868949.1:p.Gly387Ser
XM_017013462.2:c.1159G>A	XP_016868951.1:p.Gly387Ser
XM_024447163.1:c.1792G>A	XP_024302931.1:p.Gly598Ser
XM_024447164.1:c.1792G>A	XP_024302932.1:p.Gly598Ser
XM_024447165.1:c.1159G>A	XP_024302933.1:p.Gly387Ser
NM_002485.5:c.2038G>A MANE Select	NP_002476.2:p.Gly680Ser
NM_001024688.3:c.1792G>A	NP_001019859.1:p.Gly598Ser