Canonical Allele Identifier: CA2339887562

Gene: GRIN2D

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419572T= , CM000681.2:g.48419572T=	GRCh38
NC_000019.9:g.48922829T= , CM000681.1:g.48922829T=	GRCh37
NC_000019.8:g.53614641T=	NCBI36
NG_052829.1:g.29698T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.1862-13T= MANE Select	ENSP00000263269.2:n.1862-13T=
ENST00000263269.3:c.1862-13T=	ENSP00000263269.2:n.1862-13T=
NM_000836.2:c.1862-13T=	NP_000827.2:n.1862-13T=
XM_011526872.1:c.1862-13T=	XP_011525174.1:n.1862-13T=
NM_000836.4:c.1862-13T= MANE Select	NP_000827.2:n.1862-13T=