Canonical Allele Identifier: CA406697875

Gene: GRIN2D

Linked Data

• MyVariant Identifiers: chr19:g.48922903C>G (hg19) ; chr19:g.48419646C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419646C>G , CM000681.2:g.48419646C>G	GRCh38
NC_000019.9:g.48922903C>G , CM000681.1:g.48922903C>G	GRCh37
NC_000019.8:g.53614715C>G	NCBI36
NG_052829.1:g.29772C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.1923C>G MANE Select	ENSP00000263269.2:p.Phe641Leu
ENST00000263269.3:c.1923C>G	ENSP00000263269.2:p.Phe641Leu
NM_000836.2:c.1923C>G	NP_000827.2:p.Phe641Leu
XM_011526872.1:c.1923C>G	XP_011525174.1:p.Phe641Leu
NM_000836.4:c.1923C>G MANE Select	NP_000827.2:p.Phe641Leu