Canonical Allele Identifier: CA633886842
Gene: GRIN2D HGNC NCBI

Linked Data

dbSNP Id: rs1204674287
gnomAD v2: 19-48922797-TGAGAA-T
gnomAD v4: 19-48419540-TGAGAA-T
MyVariant Identifiers: chr19:g.48922798_48922802del (hg19) chr19:g.48419541_48419545del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419542_48419546del , CM000681.2:g.48419542_48419546del GRCh38
NC_000019.9:g.48922799_48922803del , CM000681.1:g.48922799_48922803del GRCh37
NC_000019.8:g.53614611_53614615del NCBI36
NG_052829.1:g.29668_29672del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1862-43_1862-39del MANE Select ENSP00000263269.2:n.1862-43_1862-39del
ENST00000263269.3:c.1862-43_1862-39del ENSP00000263269.2:n.1862-43_1862-39del
NM_000836.2:c.1862-43_1862-39del NP_000827.2:n.1862-43_1862-39del
XM_011526872.1:c.1862-43_1862-39del XP_011525174.1:n.1862-43_1862-39del
NM_000836.4:c.1862-43_1862-39del MANE Select NP_000827.2:n.1862-43_1862-39del
Search 100 bp 5'
Search 100 bp 3'