Canonical Allele Identifier: CA406698021
Gene: GRIN2D HGNC NCBI

Linked Data

dbSNP Id: rs1251679879
gnomAD v2: 19-48922929-C-T
gnomAD v3: 19-48419672-C-T
gnomAD v4: 19-48419672-C-T
MyVariant Identifiers: chr19:g.48922929C>T (hg19) chr19:g.48419672C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419672C>T , CM000681.2:g.48419672C>T GRCh38
NC_000019.9:g.48922929C>T , CM000681.1:g.48922929C>T GRCh37
NC_000019.8:g.53614741C>T NCBI36
NG_052829.1:g.29798C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1949C>T MANE Select ENSP00000263269.2:p.Pro650Leu
ENST00000263269.3:c.1949C>T ENSP00000263269.2:p.Pro650Leu
NM_000836.2:c.1949C>T NP_000827.2:p.Pro650Leu
XM_011526872.1:c.1949C>T XP_011525174.1:p.Pro650Leu
NM_000836.4:c.1949C>T MANE Select NP_000827.2:p.Pro650Leu
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