Canonical Allele Identifier: CA197290856
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs865862056
gnomAD v3: 9-101585913-A-T
gnomAD v4: 9-101585913-A-T
MyVariant Identifiers: chr9:g.104348195A>T (hg19) chr9:g.101585913A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585913A>T , CM000671.2:g.101585913A>T GRCh38
NC_000009.11:g.104348195A>T , CM000671.1:g.104348195A>T GRCh37
NC_000009.10:g.103388016A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361820.6:c.2767-6553T>A MANE Select ENSP00000355155.3:n.2767-6553T>A
ENST00000361820.3:c.2767-6553T>A ENSP00000355155.3:n.2767-6553T>A
NM_133445.2:c.2767-6553T>A NP_597702.2:n.2767-6553T>A
NM_133445.3:c.2767-6553T>A MANE Select NP_597702.2:n.2767-6553T>A
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