Canonical Allele Identifier: CA589816694
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs1357250819
gnomAD v2: 9-104348533-C-A
gnomAD v3: 9-101586251-C-A
gnomAD v4: 9-101586251-C-A
MyVariant Identifiers: chr9:g.104348533C>A (hg19) chr9:g.101586251C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101586251C>A , CM000671.2:g.101586251C>A GRCh38
NC_000009.11:g.104348533C>A , CM000671.1:g.104348533C>A GRCh37
NC_000009.10:g.103388354C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.2767-6891G>T MANE Select ENSP00000355155.3:n.2767-6891G>T
ENST00000361820.3:c.2767-6891G>T ENSP00000355155.3:n.2767-6891G>T
NM_133445.2:c.2767-6891G>T NP_597702.2:n.2767-6891G>T
NM_133445.3:c.2767-6891G>T MANE Select NP_597702.2:n.2767-6891G>T
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