Canonical Allele Identifier: CA406697969

Gene: GRIN2D

Linked Data

• MyVariant Identifiers: chr19:g.48922919G>T (hg19) ; chr19:g.48419662G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419662G>T , CM000681.2:g.48419662G>T	GRCh38
NC_000019.9:g.48922919G>T , CM000681.1:g.48922919G>T	GRCh37
NC_000019.8:g.53614731G>T	NCBI36
NG_052829.1:g.29788G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.1939G>T MANE Select	ENSP00000263269.2:p.Val647Leu
ENST00000263269.3:c.1939G>T	ENSP00000263269.2:p.Val647Leu
NM_000836.2:c.1939G>T	NP_000827.2:p.Val647Leu
XM_011526872.1:c.1939G>T	XP_011525174.1:p.Val647Leu
NM_000836.4:c.1939G>T MANE Select	NP_000827.2:p.Val647Leu