Canonical Allele Identifier: CA2017463207

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1949424571

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615429_13615431dup , CM000674.2:g.13615429_13615431dup	GRCh38
NC_000012.11:g.13768363_13768365dup , CM000674.1:g.13768363_13768365dup	GRCh37
NC_000012.10:g.13659630_13659632dup	NCBI36
NG_031854.1:g.369658_369660dup
NG_031854.2:g.371582_371584dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1500+62_1500+64dup MANE Select	ENSP00000477455.1:n.1500+62_1500+64dup
ENST00000609686.3:c.1500+62_1500+64dup	ENSP00000477455.1:n.1500+62_1500+64dup
NM_000834.3:c.1500+62_1500+64dup	NP_000825.2:n.1500+62_1500+64dup
XM_011520628.1:c.1500+62_1500+64dup	XP_011518930.1:n.1500+62_1500+64dup
XM_011520629.1:c.1500+62_1500+64dup	XP_011518931.1:n.1500+62_1500+64dup
XM_011520630.1:c.1500+62_1500+64dup	XP_011518932.1:n.1500+62_1500+64dup
XR_931372.1:n.307+203_307+205dup
XR_931373.1:n.447+203_447+205dup
XR_931374.1:n.246+203_246+205dup
NM_000834.4:c.1500+62_1500+64dup	NP_000825.2:n.1500+62_1500+64dup
XM_011520628.2:c.1500+62_1500+64dup	XP_011518930.1:n.1500+62_1500+64dup
XM_011520629.2:c.1500+62_1500+64dup	XP_011518931.1:n.1500+62_1500+64dup
XM_017019219.2:c.1500+62_1500+64dup	XP_016874708.1:n.1500+62_1500+64dup
XR_001749013.1:n.728+203_728+205dup
XR_931372.2:n.444+203_444+205dup
XR_931373.2:n.586+203_586+205dup
NM_000834.5:c.1500+62_1500+64dup MANE Select	NP_000825.2:n.1500+62_1500+64dup