Canonical Allele Identifier: CA508038140
Gene: GRIN2D HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.48922969C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419712C>G , CM000681.2:g.48419712C>G GRCh38
NC_000019.9:g.48922969C>G , CM000681.1:g.48922969C>G GRCh37
NC_000019.8:g.53614781C>G NCBI36
NG_052829.1:g.29838C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1989C>G MANE Select ENSP00000263269.2:p.Ala663=
ENST00000263269.3:c.1989C>G ENSP00000263269.2:p.Ala663=
NM_000836.2:c.1989C>G NP_000827.2:p.Ala663=
XM_011526872.1:c.1989C>G XP_011525174.1:p.Ala663=
NM_000836.4:c.1989C>G MANE Select NP_000827.2:p.Ala663=
Search 100 bp 5'
Search 100 bp 3'