Canonical Allele Identifier: CA303979790
Gene: GRIN3B HGNC NCBI

Linked Data

dbSNP Id: rs933848477
gnomAD v3: 19-1004906-C-T
gnomAD v4: 19-1004906-C-T
MyVariant Identifiers: chr19:g.1004905C>T (hg19) chr19:g.1004906C>T (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000234389.3:c.1405C>T MANE Select ENSP00000234389.3:p.Pro469Ser
ENST00000588335.1:n.155C>T
NM_138690.1:c.1405C>T NP_619635.1:p.Pro469Ser
NM_138690.2:c.1405C>T NP_619635.1:p.Pro469Ser
XM_017026243.2:c.-174C>T XP_016881732.1:n.-174C>T
NM_138690.3:c.1405C>T MANE Select NP_619635.1:p.Pro469Ser
Search 100 bp 5'
Search 100 bp 3'