Canonical Allele Identifier: CA402963952
Gene: GRIN3B HGNC NCBI

Linked Data

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

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000234389.3:c.1405C>G MANE Select ENSP00000234389.3:p.Pro469Ala
ENST00000588335.1:n.155C>G
NM_138690.1:c.1405C>G NP_619635.1:p.Pro469Ala
NM_138690.2:c.1405C>G NP_619635.1:p.Pro469Ala
XM_017026243.2:c.-174C>G XP_016881732.1:n.-174C>G
NM_138690.3:c.1405C>G MANE Select NP_619635.1:p.Pro469Ala
Search 100 bp 5'
Search 100 bp 3'