Canonical Allele Identifier: CA406697759
Gene: GRIN2D HGNC NCBI

Linked Data

dbSNP Id: rs1336648008
gnomAD v2: 19-48922877-A-G
MyVariant Identifiers: chr19:g.48922877A>G (hg19) chr19:g.48419620A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419620A>G , CM000681.2:g.48419620A>G GRCh38
NC_000019.9:g.48922877A>G , CM000681.1:g.48922877A>G GRCh37
NC_000019.8:g.53614689A>G NCBI36
NG_052829.1:g.29746A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1897A>G MANE Select ENSP00000263269.2:p.Ile633Val
ENST00000263269.3:c.1897A>G ENSP00000263269.2:p.Ile633Val
NM_000836.2:c.1897A>G NP_000827.2:p.Ile633Val
XM_011526872.1:c.1897A>G XP_011525174.1:p.Ile633Val
NM_000836.4:c.1897A>G MANE Select NP_000827.2:p.Ile633Val
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