Canonical Allele Identifier: CA478853719

Gene: GRIN2B

Linked Data

• MyVariant Identifiers: chr12:g.13906634C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13753700C>A , CM000674.2:g.13753700C>A	GRCh38
NC_000012.11:g.13906634C>A , CM000674.1:g.13906634C>A	GRCh37
NC_000012.10:g.13797901C>A	NCBI36
NG_031854.1:g.231389G>T
NG_031854.2:g.233313G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.627G>T MANE Select	ENSP00000477455.1:p.Leu209=
ENST00000630791.2:c.627G>T	ENSP00000486677.2:p.Leu209=
ENST00000609686.3:c.627G>T	ENSP00000477455.1:p.Leu209=
NM_000834.3:c.627G>T	NP_000825.2:p.Leu209=
XM_011520628.1:c.627G>T	XP_011518930.1:p.Leu209=
XM_011520629.1:c.627G>T	XP_011518931.1:p.Leu209=
XM_011520630.1:c.627G>T	XP_011518932.1:p.Leu209=
NM_000834.4:c.627G>T	NP_000825.2:p.Leu209=
XM_011520628.2:c.627G>T	XP_011518930.1:p.Leu209=
XM_011520629.2:c.627G>T	XP_011518931.1:p.Leu209=
XM_017019219.2:c.627G>T	XP_016874708.1:p.Leu209=
NM_000834.5:c.627G>T MANE Select	NP_000825.2:p.Leu209=