Canonical Allele Identifier: CA504884392
Gene: GRIN3B HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.1004901A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1004902A>C , CM000681.2:g.1004902A>C GRCh38
NC_000019.9:g.1004901A>C , CM000681.1:g.1004901A>C GRCh37
NC_000019.8:g.955901A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000234389.3:c.1401A>C MANE Select ENSP00000234389.3:p.Ser467=
ENST00000588335.1:n.151A>C
NM_138690.1:c.1401A>C NP_619635.1:p.Ser467=
NM_138690.2:c.1401A>C NP_619635.1:p.Ser467=
XM_017026243.2:c.-178A>C XP_016881732.1:n.-178A>C
NM_138690.3:c.1401A>C MANE Select NP_619635.1:p.Ser467=
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