Canonical Allele Identifier: CA2617751473

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13615373-ACATC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615374_13615377del , CM000674.2:g.13615374_13615377del	GRCh38
NC_000012.11:g.13768308_13768311del , CM000674.1:g.13768308_13768311del	GRCh37
NC_000012.10:g.13659575_13659578del	NCBI36
NG_031854.1:g.369712_369715del
NG_031854.2:g.371636_371639del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1501-110_1501-107del MANE Select	ENSP00000477455.1:n.1501-110_1501-107del
ENST00000609686.3:c.1501-110_1501-107del	ENSP00000477455.1:n.1501-110_1501-107del
NM_000834.3:c.1501-110_1501-107del	NP_000825.2:n.1501-110_1501-107del
XM_011520628.1:c.1501-110_1501-107del	XP_011518930.1:n.1501-110_1501-107del
XM_011520629.1:c.1501-110_1501-107del	XP_011518931.1:n.1501-110_1501-107del
XM_011520630.1:c.1501-110_1501-107del	XP_011518932.1:n.1501-110_1501-107del
XR_931372.1:n.307+148_307+151del
XR_931373.1:n.447+148_447+151del
XR_931374.1:n.246+148_246+151del
NM_000834.4:c.1501-110_1501-107del	NP_000825.2:n.1501-110_1501-107del
XM_011520628.2:c.1501-110_1501-107del	XP_011518930.1:n.1501-110_1501-107del
XM_011520629.2:c.1501-110_1501-107del	XP_011518931.1:n.1501-110_1501-107del
XM_017019219.2:c.1501-110_1501-107del	XP_016874708.1:n.1501-110_1501-107del
XR_001749013.1:n.728+148_728+151del
XR_931372.2:n.444+148_444+151del
XR_931373.2:n.586+148_586+151del
NM_000834.5:c.1501-110_1501-107del MANE Select	NP_000825.2:n.1501-110_1501-107del