Canonical Allele Identifier: CA402963916
Gene: GRIN3B HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.1004899T>C (hg19) chr19:g.1004900T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1004900T>C , CM000681.2:g.1004900T>C GRCh38
NC_000019.9:g.1004899T>C , CM000681.1:g.1004899T>C GRCh37
NC_000019.8:g.955899T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000234389.3:c.1399T>C MANE Select ENSP00000234389.3:p.Ser467Pro
ENST00000588335.1:n.149T>C
NM_138690.1:c.1399T>C NP_619635.1:p.Ser467Pro
NM_138690.2:c.1399T>C NP_619635.1:p.Ser467Pro
XM_017026243.2:c.-180T>C XP_016881732.1:n.-180T>C
NM_138690.3:c.1399T>C MANE Select NP_619635.1:p.Ser467Pro
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