Canonical Allele Identifier: CA197290828

Gene: GRIN3A

Linked Data

• dbSNP Id: rs1007599513
• gnomAD v2: 9-104348131-A-G
• gnomAD v3: 9-101585849-A-G
• gnomAD v4: 9-101585849-A-G
• MyVariant Identifiers: chr9:g.104348131A>G (hg19) ; chr9:g.101585849A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101585849A>G , CM000671.2:g.101585849A>G	GRCh38
NC_000009.11:g.104348131A>G , CM000671.1:g.104348131A>G	GRCh37
NC_000009.10:g.103387952A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361820.6:c.2767-6489T>C MANE Select	ENSP00000355155.3:n.2767-6489T>C
ENST00000361820.3:c.2767-6489T>C	ENSP00000355155.3:n.2767-6489T>C
NM_133445.2:c.2767-6489T>C	NP_597702.2:n.2767-6489T>C
NM_133445.3:c.2767-6489T>C MANE Select	NP_597702.2:n.2767-6489T>C