Canonical Allele Identifier: CA384052118

Gene: GRIN2B

Linked Data

• MyVariant Identifiers: chr12:g.13768467C>A (hg19) ; chr12:g.13615533C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615533C>A , CM000674.2:g.13615533C>A	GRCh38
NC_000012.11:g.13768467C>A , CM000674.1:g.13768467C>A	GRCh37
NC_000012.10:g.13659734C>A	NCBI36
NG_031854.1:g.369556G>T
NG_031854.2:g.371480G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1460G>T MANE Select	ENSP00000477455.1:p.Gly487Val
ENST00000609686.3:c.1460G>T	ENSP00000477455.1:p.Gly487Val
NM_000834.3:c.1460G>T	NP_000825.2:p.Gly487Val
XM_011520628.1:c.1460G>T	XP_011518930.1:p.Gly487Val
XM_011520629.1:c.1460G>T	XP_011518931.1:p.Gly487Val
XM_011520630.1:c.1460G>T	XP_011518932.1:p.Gly487Val
XR_931372.1:n.307+307C>A
XR_931373.1:n.447+307C>A
XR_931374.1:n.246+307C>A
NM_000834.4:c.1460G>T	NP_000825.2:p.Gly487Val
XM_011520628.2:c.1460G>T	XP_011518930.1:p.Gly487Val
XM_011520629.2:c.1460G>T	XP_011518931.1:p.Gly487Val
XM_017019219.2:c.1460G>T	XP_016874708.1:p.Gly487Val
XR_001749013.1:n.728+307C>A
XR_931372.2:n.444+307C>A
XR_931373.2:n.586+307C>A
NM_000834.5:c.1460G>T MANE Select	NP_000825.2:p.Gly487Val