Canonical Allele Identifier: CA504884389
Gene: GRIN3B HGNC NCBI

Linked Data

dbSNP Id: rs1392068595
gnomAD v2: 19-1004898-C-T
gnomAD v4: 19-1004899-C-T
MyVariant Identifiers: chr19:g.1004898C>T (hg19) chr19:g.1004899C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1004899C>T , CM000681.2:g.1004899C>T GRCh38
NC_000019.9:g.1004898C>T , CM000681.1:g.1004898C>T GRCh37
NC_000019.8:g.955898C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000234389.3:c.1398C>T MANE Select ENSP00000234389.3:p.Gly466=
ENST00000588335.1:n.148C>T
NM_138690.1:c.1398C>T NP_619635.1:p.Gly466=
NM_138690.2:c.1398C>T NP_619635.1:p.Gly466=
XM_017026243.2:c.-181C>T XP_016881732.1:n.-181C>T
NM_138690.3:c.1398C>T MANE Select NP_619635.1:p.Gly466=
Search 100 bp 5'
Search 100 bp 3'