Canonical Allele Identifier: CA996593813
Gene: GRIN2D HGNC NCBI

Linked Data

dbSNP Id: rs1262669252
gnomAD v3: 19-48419538-A-G
gnomAD v4: 19-48419538-A-G
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1862-47A>G MANE Select ENSP00000263269.2:n.1862-47A>G
ENST00000263269.3:c.1862-47A>G ENSP00000263269.2:n.1862-47A>G
NM_000836.2:c.1862-47A>G NP_000827.2:n.1862-47A>G
XM_011526872.1:c.1862-47A>G XP_011525174.1:n.1862-47A>G
NM_000836.4:c.1862-47A>G MANE Select NP_000827.2:n.1862-47A>G
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