Canonical Allele Identifier: CA856702489

Gene: NBN

Linked Data

• dbSNP Id: rs1049062648
• gnomAD v3: 8-89984424-C-G
• gnomAD v4: 8-89984424-C-G
• MyVariant Identifiers: chr8:g.90996652C>G (hg19) ; chr8:g.89984424C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.89984424C>G , CM000670.2:g.89984424C>G	GRCh38
NC_000008.10:g.90996652C>G , CM000670.1:g.90996652C>G	GRCh37
NC_000008.9:g.91065828C>G	NCBI36
NG_008860.1:g.5248G>C , LRG_158:g.5248G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000494804.2:n.141+101G>C
ENST00000523444.2:c.-260+101G>C	ENSP00000428252.2:n.-260+101G>C
ENST00000697292.1:c.37+101G>C	ENSP00000513229.1:n.37+101G>C
ENST00000697293.1:c.37+101G>C	ENSP00000513230.1:n.37+101G>C
ENST00000697294.1:c.37+101G>C	ENSP00000513231.1:n.37+101G>C
ENST00000697295.1:c.37+101G>C	ENSP00000513232.1:n.37+101G>C
ENST00000697296.1:c.37+101G>C	ENSP00000513233.1:n.37+101G>C
ENST00000697297.1:n.143+101G>C
ENST00000697298.1:c.-443+101G>C	ENSP00000513234.1:n.-443+101G>C
ENST00000697299.1:c.-76+101G>C	ENSP00000513235.1:n.-76+101G>C
ENST00000697300.1:c.-260+101G>C	ENSP00000513236.1:n.-260+101G>C
ENST00000697301.1:c.-260+101G>C	ENSP00000513237.1:n.-260+101G>C
ENST00000697302.1:c.37+101G>C	ENSP00000513238.1:n.37+101G>C
ENST00000697303.1:c.37+101G>C	ENSP00000513239.1:n.37+101G>C
ENST00000697304.1:c.37+101G>C	ENSP00000513240.1:n.37+101G>C
ENST00000697306.1:c.37+101G>C	ENSP00000513241.1:n.37+101G>C
ENST00000697307.1:c.37+101G>C	ENSP00000513242.1:n.37+101G>C
ENST00000697308.1:c.37+101G>C	ENSP00000513243.1:n.37+101G>C
ENST00000697309.1:c.37+101G>C	ENSP00000513244.1:n.37+101G>C
ENST00000697310.1:c.37+101G>C	ENSP00000513245.1:n.37+101G>C
ENST00000697311.1:c.37+101G>C	ENSP00000513246.1:n.37+101G>C
ENST00000697312.1:c.37+101G>C	ENSP00000513247.1:n.37+101G>C
ENST00000697313.1:n.149+101G>C
ENST00000697314.1:n.149+101G>C
ENST00000697315.1:c.37+101G>C	ENSP00000513248.1:n.37+101G>C
ENST00000697316.1:n.158+101G>C
ENST00000697317.1:n.147+101G>C
ENST00000697318.1:n.149+101G>C
ENST00000265433.8:c.37+101G>C MANE Select	ENSP00000265433.4:n.37+101G>C
ENST00000265433.7:c.37+101G>C	ENSP00000265433.3:n.37+101G>C
ENST00000396252.6:c.37+101G>C	ENSP00000379551.2:n.37+101G>C
ENST00000494804.1:n.141+101G>C
ENST00000519426.5:c.37+101G>C	ENSP00000430983.1:n.37+101G>C
ENST00000523444.1:c.37+101G>C	ENSP00000428252.1:n.37+101G>C
NM_001024688.2:c.-260+101G>C	NP_001019859.1:n.-260+101G>C
NM_002485.4:c.37+101G>C , LRG_158t1:c.37+101G>C	NP_002476.2:n.37+101G>C
XM_011517046.1:c.37+101G>C	XP_011515348.1:n.37+101G>C
XR_928335.1:n.174+101G>C
XM_017013460.1:c.-983+101G>C	XP_016868949.1:n.-983+101G>C
XM_017013462.2:c.-789+101G>C	XP_016868951.1:n.-789+101G>C
XM_024447165.1:c.-933+101G>C	XP_024302933.1:n.-933+101G>C
NM_002485.5:c.37+101G>C MANE Select	NP_002476.2:n.37+101G>C
NM_001024688.3:c.-260+101G>C	NP_001019859.1:n.-260+101G>C