Canonical Allele Identifier: CA857768728

Gene: GRIN3A

Linked Data

• dbSNP Id: rs1459816857
• gnomAD v3: 9-101585735-C-T
• gnomAD v4: 9-101585735-C-T
• MyVariant Identifiers: chr9:g.104348017C>T (hg19) ; chr9:g.101585735C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101585735C>T , CM000671.2:g.101585735C>T	GRCh38
NC_000009.11:g.104348017C>T , CM000671.1:g.104348017C>T	GRCh37
NC_000009.10:g.103387838C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361820.6:c.2767-6375G>A MANE Select	ENSP00000355155.3:n.2767-6375G>A
ENST00000361820.3:c.2767-6375G>A	ENSP00000355155.3:n.2767-6375G>A
NM_133445.2:c.2767-6375G>A	NP_597702.2:n.2767-6375G>A
NM_133445.3:c.2767-6375G>A MANE Select	NP_597702.2:n.2767-6375G>A