Canonical Allele Identifier: CA402963950
Gene: GRIN3B HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.1004905C>A (hg19) chr19:g.1004906C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1004906C>A , CM000681.2:g.1004906C>A GRCh38
NC_000019.9:g.1004905C>A , CM000681.1:g.1004905C>A GRCh37
NC_000019.8:g.955905C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000234389.3:c.1405C>A MANE Select ENSP00000234389.3:p.Pro469Thr
ENST00000588335.1:n.155C>A
NM_138690.1:c.1405C>A NP_619635.1:p.Pro469Thr
NM_138690.2:c.1405C>A NP_619635.1:p.Pro469Thr
XM_017026243.2:c.-174C>A XP_016881732.1:n.-174C>A
NM_138690.3:c.1405C>A MANE Select NP_619635.1:p.Pro469Thr
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