Canonical Allele Identifier: CA857768767
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs1183935080
gnomAD v3: 9-101585817-TG-T
gnomAD v4: 9-101585817-TG-T
MyVariant Identifiers: chr9:g.104348100del (hg19) chr9:g.101585818del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585818del , CM000671.2:g.101585818del GRCh38
NC_000009.11:g.104348100del , CM000671.1:g.104348100del GRCh37
NC_000009.10:g.103387921del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.2767-6458del MANE Select ENSP00000355155.3:n.2767-6458del
ENST00000361820.3:c.2767-6458del ENSP00000355155.3:n.2767-6458del
NM_133445.2:c.2767-6458del NP_597702.2:n.2767-6458del
NM_133445.3:c.2767-6458del MANE Select NP_597702.2:n.2767-6458del
Search 100 bp 5'
Search 100 bp 3'