Canonical Allele Identifier: CA944929887

Gene: GRIN2B

Linked Data

• gnomAD v3: 12-13562374-A-AAAAGCTAAAGAGGCTATGTGAGCACAAAGGTAGCTTTCACCTAAATGAAAAGATCC
• gnomAD v4: 12-13562374-A-AAAAGCTAAAGAGGCTATGTGAGCACAAAGGTAGCTTTCACCTAAATGAAAAGATCC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562374_13562375insAAAGCTAAAGAGGCTATGTGAGCACAAAGGTAGCTTTCACCTAAATGAAAAGATCC , CM000674.2:g.13562374_13562375insAAAGCTAAAGAGGCTATGTGAGCACAAAGGTAGCTTTCACCTAAATGAAAAGATCC	GRCh38
NC_000012.11:g.13715308_13715309insAAAGCTAAAGAGGCTATGTGAGCACAAAGGTAGCTTTCACCTAAATGAAAAGATCC , CM000674.1:g.13715308_13715309insAAAGCTAAAGAGGCTATGTGAGCACAAAGGTAGCTTTCACCTAAATGAAAAGATCC	GRCh37
NC_000012.10:g.13606575_13606576insAAAGCTAAAGAGGCTATGTGAGCACAAAGGTAGCTTTCACCTAAATGAAAAGATCC	NCBI36
NG_031854.1:g.422714_422715insGGATCTTTTCATTTAGGTGAAAGCTACCTTTGTGCTCACATAGCCTCTTTAGCTTT
NG_031854.2:g.424638_424639insGGATCTTTTCATTTAGGTGAAAGCTACCTTTGTGCTCACATAGCCTCTTTAGCTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.*408_*409insGGATCTTTTCATTTAGGTGAAAGCTACCTTTGTGCTCACATAGCCTCTTTAGCTTT MANE Select	ENSP00000477455.1:n.*408_*409insGGATCTTTT...
ENST00000637214.1:c.69+46228_69+46229insGGATCTTTTCATTTAGGTGAAAGCTACCTTTGTGCTCACATAGCCTCTTTAGCTTT	ENSP00000489997.1:n.69+46228_69+46229insG...
ENST00000609686.3:c.*408_*409insGGATCTTTTCATTTAGGTGAAAGCTACCTTTGTGCTCACATAGCCTCTTTAGCTTT	ENSP00000477455.1:n.*408_*409insGGATCTTTT...
NM_000834.3:c.*408_*409insGGATCTTTTCATTTAGGTGAAAGCTACCTTTGTGCTCACATAGCCTCTTTAGCTTT	NP_000825.2:n.*408_*409insGGATCTTTTCATTTA...
XM_005253351.2:c.*408_*409insGGATCTTTTCATTTAGGTGAAAGCTACCTTTGTGCTCACATAGCCTCTTTAGCTTT	XP_005253408.1:n.*408_*409insGGATCTTTTCAT...
XM_011520628.1:c.*408_*409insGGATCTTTTCATTTAGGTGAAAGCTACCTTTGTGCTCACATAGCCTCTTTAGCTTT	XP_011518930.1:n.*408_*409insGGATCTTTTCAT...
XM_011520629.1:c.*408_*409insGGATCTTTTCATTTAGGTGAAAGCTACCTTTGTGCTCACATAGCCTCTTTAGCTTT	XP_011518931.1:n.*408_*409insGGATCTTTTCAT...
XM_011520630.1:c.*408_*409insGGATCTTTTCATTTAGGTGAAAGCTACCTTTGTGCTCACATAGCCTCTTTAGCTTT	XP_011518932.1:n.*408_*409insGGATCTTTTCAT...
NM_000834.4:c.*408_*409insGGATCTTTTCATTTAGGTGAAAGCTACCTTTGTGCTCACATAGCCTCTTTAGCTTT	NP_000825.2:n.*408_*409insGGATCTTTTCATTTA...
XM_005253351.3:c.*408_*409insGGATCTTTTCATTTAGGTGAAAGCTACCTTTGTGCTCACATAGCCTCTTTAGCTTT	XP_005253408.1:n.*408_*409insGGATCTTTTCAT...
XM_011520628.2:c.*408_*409insGGATCTTTTCATTTAGGTGAAAGCTACCTTTGTGCTCACATAGCCTCTTTAGCTTT	XP_011518930.1:n.*408_*409insGGATCTTTTCAT...
XM_011520629.2:c.*408_*409insGGATCTTTTCATTTAGGTGAAAGCTACCTTTGTGCTCACATAGCCTCTTTAGCTTT	XP_011518931.1:n.*408_*409insGGATCTTTTCAT...
XM_017019219.2:c.*408_*409insGGATCTTTTCATTTAGGTGAAAGCTACCTTTGTGCTCACATAGCCTCTTTAGCTTT	XP_016874708.1:n.*408_*409insGGATCTTTTCAT...
NM_000834.5:c.*408_*409insGGATCTTTTCATTTAGGTGAAAGCTACCTTTGTGCTCACATAGCCTCTTTAGCTTT MANE Select	NP_000825.2:n.*408_*409insGGATCTTTTCATTTA...