Canonical Allele Identifier: CA857768832
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs1164049546
MyVariant Identifiers: chr9:g.104348212_104348214del (hg19) chr9:g.101585930_101585932del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585935_101585937del , CM000671.2:g.101585935_101585937del GRCh38
NC_000009.11:g.104348217_104348219del , CM000671.1:g.104348217_104348219del GRCh37
NC_000009.10:g.103388038_103388040del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.2767-6572_2767-6570del MANE Select ENSP00000355155.3:n.2767-6572_2767-6570del
ENST00000361820.3:c.2767-6572_2767-6570del ENSP00000355155.3:n.2767-6572_2767-6570del
NM_133445.2:c.2767-6572_2767-6570del NP_597702.2:n.2767-6572_2767-6570del
NM_133445.3:c.2767-6572_2767-6570del MANE Select NP_597702.2:n.2767-6572_2767-6570del
Search 100 bp 5'
Search 100 bp 3'