Canonical Allele Identifier: CA478853838

Gene: GRIN2B

Linked Data

• COSMIC: COSM2002795
• MyVariant Identifiers: chr12:g.13906733G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13753799G>A , CM000674.2:g.13753799G>A	GRCh38
NC_000012.11:g.13906733G>A , CM000674.1:g.13906733G>A	GRCh37
NC_000012.10:g.13798000G>A	NCBI36
NG_031854.1:g.231290C>T
NG_031854.2:g.233214C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.528C>T MANE Select	ENSP00000477455.1:p.Phe176=
ENST00000630791.2:c.528C>T	ENSP00000486677.2:p.Phe176=
ENST00000609686.3:c.528C>T	ENSP00000477455.1:p.Phe176=
NM_000834.3:c.528C>T	NP_000825.2:p.Phe176=
XM_011520628.1:c.528C>T	XP_011518930.1:p.Phe176=
XM_011520629.1:c.528C>T	XP_011518931.1:p.Phe176=
XM_011520630.1:c.528C>T	XP_011518932.1:p.Phe176=
NM_000834.4:c.528C>T	NP_000825.2:p.Phe176=
XM_011520628.2:c.528C>T	XP_011518930.1:p.Phe176=
XM_011520629.2:c.528C>T	XP_011518931.1:p.Phe176=
XM_017019219.2:c.528C>T	XP_016874708.1:p.Phe176=
NM_000834.5:c.528C>T MANE Select	NP_000825.2:p.Phe176=