Canonical Allele Identifier: CA2586189532
Gene: GRIN2D HGNC NCBI

Linked Data

gnomAD v4: 19-48419506-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419506T>G , CM000681.2:g.48419506T>G GRCh38
NC_000019.9:g.48922763T>G , CM000681.1:g.48922763T>G GRCh37
NC_000019.8:g.53614575T>G NCBI36
NG_052829.1:g.29632T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1862-79T>G MANE Select ENSP00000263269.2:n.1862-79T>G
ENST00000263269.3:c.1862-79T>G ENSP00000263269.2:n.1862-79T>G
NM_000836.2:c.1862-79T>G NP_000827.2:n.1862-79T>G
XM_011526872.1:c.1862-79T>G XP_011525174.1:n.1862-79T>G
NM_000836.4:c.1862-79T>G MANE Select NP_000827.2:n.1862-79T>G
Search 100 bp 5'
Search 100 bp 3'