Canonical Allele Identifier: CA633886841
Gene: GRIN2D HGNC NCBI

Linked Data

dbSNP Id: rs1262669252
gnomAD v2: 19-48922795-A-T
gnomAD v3: 19-48419538-A-T
gnomAD v4: 19-48419538-A-T
MyVariant Identifiers: chr19:g.48922795A>T (hg19) chr19:g.48419538A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419538A>T , CM000681.2:g.48419538A>T GRCh38
NC_000019.9:g.48922795A>T , CM000681.1:g.48922795A>T GRCh37
NC_000019.8:g.53614607A>T NCBI36
NG_052829.1:g.29664A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1862-47A>T MANE Select ENSP00000263269.2:n.1862-47A>T
ENST00000263269.3:c.1862-47A>T ENSP00000263269.2:n.1862-47A>T
NM_000836.2:c.1862-47A>T NP_000827.2:n.1862-47A>T
XM_011526872.1:c.1862-47A>T XP_011525174.1:n.1862-47A>T
NM_000836.4:c.1862-47A>T MANE Select NP_000827.2:n.1862-47A>T
Search 100 bp 5'
Search 100 bp 3'