Canonical Allele Identifier: CA2586189569
Gene: GRIN2D HGNC NCBI

Linked Data

gnomAD v4: 19-48419533-T-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419533T>A , CM000681.2:g.48419533T>A GRCh38
NC_000019.9:g.48922790T>A , CM000681.1:g.48922790T>A GRCh37
NC_000019.8:g.53614602T>A NCBI36
NG_052829.1:g.29659T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1862-52T>A MANE Select ENSP00000263269.2:n.1862-52T>A
ENST00000263269.3:c.1862-52T>A ENSP00000263269.2:n.1862-52T>A
NM_000836.2:c.1862-52T>A NP_000827.2:n.1862-52T>A
XM_011526872.1:c.1862-52T>A XP_011525174.1:n.1862-52T>A
NM_000836.4:c.1862-52T>A MANE Select NP_000827.2:n.1862-52T>A
Search 100 bp 5'
Search 100 bp 3'