Canonical Allele Identifier: CA857768838

Gene: GRIN3A

Linked Data

• dbSNP Id: rs1470449440
• gnomAD v3: 9-101585943-G-A
• gnomAD v4: 9-101585943-G-A
• MyVariant Identifiers: chr9:g.104348225G>A (hg19) ; chr9:g.101585943G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.101585943G>A , CM000671.2:g.101585943G>A	GRCh38
NC_000009.11:g.104348225G>A , CM000671.1:g.104348225G>A	GRCh37
NC_000009.10:g.103388046G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361820.6:c.2767-6583C>T MANE Select	ENSP00000355155.3:n.2767-6583C>T
ENST00000361820.3:c.2767-6583C>T	ENSP00000355155.3:n.2767-6583C>T
NM_133445.2:c.2767-6583C>T	NP_597702.2:n.2767-6583C>T
NM_133445.3:c.2767-6583C>T MANE Select	NP_597702.2:n.2767-6583C>T