Canonical Allele Identifier: CA406698384

Gene: GRIN2D

Linked Data

• MyVariant Identifiers: chr19:g.48923036T>C (hg19) ; chr19:g.48419779T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419779T>C , CM000681.2:g.48419779T>C	GRCh38
NC_000019.9:g.48923036T>C , CM000681.1:g.48923036T>C	GRCh37
NC_000019.8:g.53614848T>C	NCBI36
NG_052829.1:g.29905T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.2056T>C MANE Select	ENSP00000263269.2:p.Tyr686His
ENST00000263269.3:c.2056T>C	ENSP00000263269.2:p.Tyr686His
NM_000836.2:c.2056T>C	NP_000827.2:p.Tyr686His
XM_011526872.1:c.2056T>C	XP_011525174.1:p.Tyr686His
NM_000836.4:c.2056T>C MANE Select	NP_000827.2:p.Tyr686His