Canonical Allele Identifier: CA197291011
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs764475746
MyVariant Identifiers: chr9:g.104348558T>A (hg19) chr9:g.101586276T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101586276T>A , CM000671.2:g.101586276T>A GRCh38
NC_000009.11:g.104348558T>A , CM000671.1:g.104348558T>A GRCh37
NC_000009.10:g.103388379T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.2767-6916A>T MANE Select ENSP00000355155.3:n.2767-6916A>T
ENST00000361820.3:c.2767-6916A>T ENSP00000355155.3:n.2767-6916A>T
NM_133445.2:c.2767-6916A>T NP_597702.2:n.2767-6916A>T
NM_133445.3:c.2767-6916A>T MANE Select NP_597702.2:n.2767-6916A>T
Search 100 bp 5'
Search 100 bp 3'