Canonical Allele Identifier: CA508038080
Gene: GRIN2D HGNC NCBI

Linked Data

dbSNP Id: rs1792607799
MyVariant Identifiers: chr19:g.48922876C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419619C>G , CM000681.2:g.48419619C>G GRCh38
NC_000019.9:g.48922876C>G , CM000681.1:g.48922876C>G GRCh37
NC_000019.8:g.53614688C>G NCBI36
NG_052829.1:g.29745C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1896C>G MANE Select ENSP00000263269.2:p.Ser632=
ENST00000263269.3:c.1896C>G ENSP00000263269.2:p.Ser632=
NM_000836.2:c.1896C>G NP_000827.2:p.Ser632=
XM_011526872.1:c.1896C>G XP_011525174.1:p.Ser632=
NM_000836.4:c.1896C>G MANE Select NP_000827.2:p.Ser632=
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