Canonical Allele Identifier: CA406697929
Gene: GRIN2D HGNC NCBI

Linked Data

gnomAD v4: 19-48419654-C-T
COSMIC: COSM998959
MyVariant Identifiers: chr19:g.48922911C>T (hg19) chr19:g.48419654C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419654C>T , CM000681.2:g.48419654C>T GRCh38
NC_000019.9:g.48922911C>T , CM000681.1:g.48922911C>T GRCh37
NC_000019.8:g.53614723C>T NCBI36
NG_052829.1:g.29780C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1931C>T MANE Select ENSP00000263269.2:p.Ser644Leu
ENST00000263269.3:c.1931C>T ENSP00000263269.2:p.Ser644Leu
NM_000836.2:c.1931C>T NP_000827.2:p.Ser644Leu
XM_011526872.1:c.1931C>T XP_011525174.1:p.Ser644Leu
NM_000836.4:c.1931C>T MANE Select NP_000827.2:p.Ser644Leu
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