Canonical Allele Identifier: CA402963905
Gene: GRIN3B HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.1004897G>A (hg19) chr19:g.1004898G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1004898G>A , CM000681.2:g.1004898G>A GRCh38
NC_000019.9:g.1004897G>A , CM000681.1:g.1004897G>A GRCh37
NC_000019.8:g.955897G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000234389.3:c.1397G>A MANE Select ENSP00000234389.3:p.Gly466Asp
ENST00000588335.1:n.147G>A
NM_138690.1:c.1397G>A NP_619635.1:p.Gly466Asp
NM_138690.2:c.1397G>A NP_619635.1:p.Gly466Asp
XM_017026243.2:c.-182G>A XP_016881732.1:n.-182G>A
NM_138690.3:c.1397G>A MANE Select NP_619635.1:p.Gly466Asp
Search 100 bp 5'
Search 100 bp 3'