Canonical Allele Identifier: CA508038128

Gene: GRIN2D

Linked Data

• MyVariant Identifiers: chr19:g.48922951C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419694C>T , CM000681.2:g.48419694C>T	GRCh38
NC_000019.9:g.48922951C>T , CM000681.1:g.48922951C>T	GRCh37
NC_000019.8:g.53614763C>T	NCBI36
NG_052829.1:g.29820C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.1971C>T MANE Select	ENSP00000263269.2:p.Ile657=
ENST00000263269.3:c.1971C>T	ENSP00000263269.2:p.Ile657=
NM_000836.2:c.1971C>T	NP_000827.2:p.Ile657=
XM_011526872.1:c.1971C>T	XP_011525174.1:p.Ile657=
NM_000836.4:c.1971C>T MANE Select	NP_000827.2:p.Ile657=