Canonical Allele Identifier: CA944960871

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1867332115
• gnomAD v3: 12-13944715-G-GT
• gnomAD v4: 12-13944715-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13944715_13944716insT , CM000674.2:g.13944715_13944716insT	GRCh38
NC_000012.11:g.14097649_14097650insT , CM000674.1:g.14097649_14097650insT	GRCh37
NC_000012.10:g.13988916_13988917insT	NCBI36
NG_031854.1:g.40373_40374insA
NG_031854.2:g.42297_42298insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.-19+35212_-19+35213insA MANE Select	ENSP00000477455.1:n.-19+35212_-19+35213insA
ENST00000630791.2:c.-19+35212_-19+35213insA	ENSP00000486677.2:n.-19+35212_-19+35213insA
ENST00000609686.3:c.-19+35212_-19+35213insA	ENSP00000477455.1:n.-19+35212_-19+35213insA
ENST00000627535.2:c.-19+35212_-19+35213insA	ENSP00000486411.1:n.-19+35212_-19+35213insA
ENST00000630791.1:c.-19+35212_-19+35213insA	ENSP00000486677.1:n.-19+35212_-19+35213insA
NM_000834.3:c.-19+35212_-19+35213insA	NP_000825.2:n.-19+35212_-19+35213insA
XM_011520628.1:c.-19+35212_-19+35213insA	XP_011518930.1:n.-19+35212_-19+35213insA
XM_011520629.1:c.-19+35212_-19+35213insA	XP_011518931.1:n.-19+35212_-19+35213insA
XM_011520630.1:c.-19+35212_-19+35213insA	XP_011518932.1:n.-19+35212_-19+35213insA
NM_000834.4:c.-19+35212_-19+35213insA	NP_000825.2:n.-19+35212_-19+35213insA
XM_011520628.2:c.-19+35212_-19+35213insA	XP_011518930.1:n.-19+35212_-19+35213insA
XM_011520629.2:c.-19+35212_-19+35213insA	XP_011518931.1:n.-19+35212_-19+35213insA
XM_017019219.2:c.-19+35212_-19+35213insA	XP_016874708.1:n.-19+35212_-19+35213insA
NM_000834.5:c.-19+35212_-19+35213insA MANE Select	NP_000825.2:n.-19+35212_-19+35213insA