Canonical Allele Identifier: CA883006291
Gene: GRIN2D HGNC NCBI

Linked Data

dbSNP Id: rs1177785671
gnomAD v3: 19-48419529-CCCTT-C
gnomAD v4: 19-48419529-CCCTT-C
MyVariant Identifiers: chr19:g.48922787_48922790del (hg19) chr19:g.48419530_48419533del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419534_48419537del , CM000681.2:g.48419534_48419537del GRCh38
NC_000019.9:g.48922791_48922794del , CM000681.1:g.48922791_48922794del GRCh37
NC_000019.8:g.53614603_53614606del NCBI36
NG_052829.1:g.29660_29663del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1862-51_1862-48del MANE Select ENSP00000263269.2:n.1862-51_1862-48del
ENST00000263269.3:c.1862-51_1862-48del ENSP00000263269.2:n.1862-51_1862-48del
NM_000836.2:c.1862-51_1862-48del NP_000827.2:n.1862-51_1862-48del
XM_011526872.1:c.1862-51_1862-48del XP_011525174.1:n.1862-51_1862-48del
NM_000836.4:c.1862-51_1862-48del MANE Select NP_000827.2:n.1862-51_1862-48del
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