Canonical Allele Identifier: CA2814655031

Gene: GRIN2D

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419527T>G , CM000681.2:g.48419527T>G	GRCh38
NC_000019.9:g.48922784T>G , CM000681.1:g.48922784T>G	GRCh37
NC_000019.8:g.53614596T>G	NCBI36
NG_052829.1:g.29653T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.1862-58T>G MANE Select	ENSP00000263269.2:n.1862-58T>G
ENST00000263269.3:c.1862-58T>G	ENSP00000263269.2:n.1862-58T>G
NM_000836.2:c.1862-58T>G	NP_000827.2:n.1862-58T>G
XM_011526872.1:c.1862-58T>G	XP_011525174.1:n.1862-58T>G
NM_000836.4:c.1862-58T>G MANE Select	NP_000827.2:n.1862-58T>G