Canonical Allele Identifier: CA603450256

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1321096561
• gnomAD v2: 12-13768203-T-TA
• gnomAD v4: 12-13615269-T-TA
• MyVariant Identifiers: chr12:g.13768203_13768204insA (hg19) ; chr12:g.13615269_13615270insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615273dup , CM000674.2:g.13615273dup	GRCh38
NC_000012.11:g.13768207dup , CM000674.1:g.13768207dup	GRCh37
NC_000012.10:g.13659474dup	NCBI36
NG_031854.1:g.369819dup
NG_031854.2:g.371743dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1501-3dup MANE Select	ENSP00000477455.1:n.1501-3dup
ENST00000609686.3:c.1501-3dup	ENSP00000477455.1:n.1501-3dup
NM_000834.3:c.1501-3dup	NP_000825.2:n.1501-3dup
XM_011520628.1:c.1501-3dup	XP_011518930.1:n.1501-3dup
XM_011520629.1:c.1501-3dup	XP_011518931.1:n.1501-3dup
XM_011520630.1:c.1501-3dup	XP_011518932.1:n.1501-3dup
XR_931372.1:n.307+47dup
XR_931373.1:n.447+47dup
XR_931374.1:n.246+47dup
NM_000834.4:c.1501-3dup	NP_000825.2:n.1501-3dup
XM_011520628.2:c.1501-3dup	XP_011518930.1:n.1501-3dup
XM_011520629.2:c.1501-3dup	XP_011518931.1:n.1501-3dup
XM_017019219.2:c.1501-3dup	XP_016874708.1:n.1501-3dup
XR_001749013.1:n.728+47dup
XR_931372.2:n.444+47dup
XR_931373.2:n.586+47dup
NM_000834.5:c.1501-3dup MANE Select	NP_000825.2:n.1501-3dup