Canonical Allele Identifier: CA9550626

Gene: GRIN2D

Linked Data

• dbSNP Id: rs752875753
• ExAC: 19:48922912 G / A
• gnomAD v2: 19-48922912-G-A
• gnomAD v3: 19-48419655-G-A
• gnomAD v4: 19-48419655-G-A
• MyVariant Identifiers: chr19:g.48922912G>A (hg19) ; chr19:g.48419655G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419655G>A , CM000681.2:g.48419655G>A	GRCh38
NC_000019.9:g.48922912G>A , CM000681.1:g.48922912G>A	GRCh37
NC_000019.8:g.53614724G>A	NCBI36
NG_052829.1:g.29781G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.1932G>A MANE Select	ENSP00000263269.2:p.Ser644=
ENST00000263269.3:c.1932G>A	ENSP00000263269.2:p.Ser644=
NM_000836.2:c.1932G>A	NP_000827.2:p.Ser644=
XM_011526872.1:c.1932G>A	XP_011525174.1:p.Ser644=
NM_000836.4:c.1932G>A MANE Select	NP_000827.2:p.Ser644=