Canonical Allele Identifier: CA384053477

Gene: GRIN2B

Linked Data

• MyVariant Identifiers: chr12:g.13906474C>T (hg19) ; chr12:g.13753540C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13753540C>T , CM000674.2:g.13753540C>T	GRCh38
NC_000012.11:g.13906474C>T , CM000674.1:g.13906474C>T	GRCh37
NC_000012.10:g.13797741C>T	NCBI36
NG_031854.1:g.231549G>A
NG_031854.2:g.233473G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.787G>A MANE Select	ENSP00000477455.1:p.Ala263Thr
ENST00000630791.2:c.787G>A	ENSP00000486677.2:p.Ala263Thr
ENST00000609686.3:c.787G>A	ENSP00000477455.1:p.Ala263Thr
NM_000834.3:c.787G>A	NP_000825.2:p.Ala263Thr
XM_011520628.1:c.787G>A	XP_011518930.1:p.Ala263Thr
XM_011520629.1:c.787G>A	XP_011518931.1:p.Ala263Thr
XM_011520630.1:c.787G>A	XP_011518932.1:p.Ala263Thr
NM_000834.4:c.787G>A	NP_000825.2:p.Ala263Thr
XM_011520628.2:c.787G>A	XP_011518930.1:p.Ala263Thr
XM_011520629.2:c.787G>A	XP_011518931.1:p.Ala263Thr
XM_017019219.2:c.787G>A	XP_016874708.1:p.Ala263Thr
NM_000834.5:c.787G>A MANE Select	NP_000825.2:p.Ala263Thr