Canonical Allele Identifier: CA633886833
Gene: GRIN2D HGNC NCBI

Linked Data

dbSNP Id: rs11302654
gnomAD v2: 19-48922772-CTTT-C
gnomAD v3: 19-48419515-CTTT-C
gnomAD v4: 19-48419515-CTTT-C
MyVariant Identifiers: chr19:g.48922773_48922775del (hg19) chr19:g.48419516_48419518del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419526_48419528del , CM000681.2:g.48419526_48419528del GRCh38
NC_000019.9:g.48922783_48922785del , CM000681.1:g.48922783_48922785del GRCh37
NC_000019.8:g.53614595_53614597del NCBI36
NG_052829.1:g.29652_29654del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1862-59_1862-57del MANE Select ENSP00000263269.2:n.1862-59_1862-57del
ENST00000263269.3:c.1862-59_1862-57del ENSP00000263269.2:n.1862-59_1862-57del
NM_000836.2:c.1862-59_1862-57del NP_000827.2:n.1862-59_1862-57del
XM_011526872.1:c.1862-59_1862-57del XP_011525174.1:n.1862-59_1862-57del
NM_000836.4:c.1862-59_1862-57del MANE Select NP_000827.2:n.1862-59_1862-57del
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