Canonical Allele Identifier: CA478771334

Gene: GRIN2B

Linked Data

• MyVariant Identifiers: chr12:g.13761606A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608672A>T , CM000674.2:g.13608672A>T	GRCh38
NC_000012.11:g.13761606A>T , CM000674.1:g.13761606A>T	GRCh37
NC_000012.10:g.13652873A>T	NCBI36
NG_031854.1:g.376417T>A
NG_031854.2:g.378341T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1941T>A MANE Select	ENSP00000477455.1:p.Thr647=
ENST00000628166.2:n.201T>A
ENST00000609686.3:c.1941T>A	ENSP00000477455.1:p.Thr647=
ENST00000628166.1:n.201T>A
NM_000834.3:c.1941T>A	NP_000825.2:p.Thr647=
XM_005253351.2:c.-113T>A	XP_005253408.1:n.-113T>A
XM_011520628.1:c.1941T>A	XP_011518930.1:p.Thr647=
XM_011520629.1:c.1941T>A	XP_011518931.1:p.Thr647=
XM_011520630.1:c.1941T>A	XP_011518932.1:p.Thr647=
XR_931372.1:n.179-6426A>T
XR_931373.1:n.233A>T
NM_000834.4:c.1941T>A	NP_000825.2:p.Thr647=
XM_005253351.3:c.-113T>A	XP_005253408.1:n.-113T>A
XM_011520628.2:c.1941T>A	XP_011518930.1:p.Thr647=
XM_011520629.2:c.1941T>A	XP_011518931.1:p.Thr647=
XM_017019219.2:c.1941T>A	XP_016874708.1:p.Thr647=
XR_001749013.1:n.372A>T
XR_931372.2:n.316-6426A>T
XR_931373.2:n.372A>T
NM_000834.5:c.1941T>A MANE Select	NP_000825.2:p.Thr647=