Canonical Allele Identifier: CA406697885

Gene: GRIN2D

Linked Data

• MyVariant Identifiers: chr19:g.48922905A>G (hg19) ; chr19:g.48419648A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419648A>G , CM000681.2:g.48419648A>G	GRCh38
NC_000019.9:g.48922905A>G , CM000681.1:g.48922905A>G	GRCh37
NC_000019.8:g.53614717A>G	NCBI36
NG_052829.1:g.29774A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000263269.4:c.1925A>G MANE Select	ENSP00000263269.2:p.Asn642Ser
ENST00000263269.3:c.1925A>G	ENSP00000263269.2:p.Asn642Ser
NM_000836.2:c.1925A>G	NP_000827.2:p.Asn642Ser
XM_011526872.1:c.1925A>G	XP_011525174.1:p.Asn642Ser
NM_000836.4:c.1925A>G MANE Select	NP_000827.2:p.Asn642Ser