Canonical Allele Identifier: CA2339887520

Gene: GRIN2D

Linked Data

• dbSNP Id: rs1600982009

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419495A>C , CM000681.2:g.48419495A>C	GRCh38
NC_000019.9:g.48922752A>C , CM000681.1:g.48922752A>C	GRCh37
NC_000019.8:g.53614564A>C	NCBI36
NG_052829.1:g.29621A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.1862-90A>C MANE Select	ENSP00000263269.2:n.1862-90A>C
ENST00000263269.3:c.1862-90A>C	ENSP00000263269.2:n.1862-90A>C
NM_000836.2:c.1862-90A>C	NP_000827.2:n.1862-90A>C
XM_011526872.1:c.1862-90A>C	XP_011525174.1:n.1862-90A>C
NM_000836.4:c.1862-90A>C MANE Select	NP_000827.2:n.1862-90A>C