Canonical Allele Identifier: CA2617751557

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13615451-T-TAAATGA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615457_13615462dup , CM000674.2:g.13615457_13615462dup	GRCh38
NC_000012.11:g.13768391_13768396dup , CM000674.1:g.13768391_13768396dup	GRCh37
NC_000012.10:g.13659658_13659663dup	NCBI36
NG_031854.1:g.369632_369637dup
NG_031854.2:g.371556_371561dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1500+36_1500+41dup MANE Select	ENSP00000477455.1:n.1500+36_1500+41dup
ENST00000609686.3:c.1500+36_1500+41dup	ENSP00000477455.1:n.1500+36_1500+41dup
NM_000834.3:c.1500+36_1500+41dup	NP_000825.2:n.1500+36_1500+41dup
XM_011520628.1:c.1500+36_1500+41dup	XP_011518930.1:n.1500+36_1500+41dup
XM_011520629.1:c.1500+36_1500+41dup	XP_011518931.1:n.1500+36_1500+41dup
XM_011520630.1:c.1500+36_1500+41dup	XP_011518932.1:n.1500+36_1500+41dup
XR_931372.1:n.307+231_307+236dup
XR_931373.1:n.447+231_447+236dup
XR_931374.1:n.246+231_246+236dup
NM_000834.4:c.1500+36_1500+41dup	NP_000825.2:n.1500+36_1500+41dup
XM_011520628.2:c.1500+36_1500+41dup	XP_011518930.1:n.1500+36_1500+41dup
XM_011520629.2:c.1500+36_1500+41dup	XP_011518931.1:n.1500+36_1500+41dup
XM_017019219.2:c.1500+36_1500+41dup	XP_016874708.1:n.1500+36_1500+41dup
XR_001749013.1:n.728+231_728+236dup
XR_931372.2:n.444+231_444+236dup
XR_931373.2:n.586+231_586+236dup
NM_000834.5:c.1500+36_1500+41dup MANE Select	NP_000825.2:n.1500+36_1500+41dup