Canonical Allele Identifier: CA374271682
Gene: GRIN3A HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.104449109T>C (hg19) chr9:g.101686827T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101686827T>C , CM000671.2:g.101686827T>C GRCh38
NC_000009.11:g.104449109T>C , CM000671.1:g.104449109T>C GRCh37
NC_000009.10:g.103488930T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361820.6:c.1073A>G MANE Select ENSP00000355155.3:p.Asp358Gly
ENST00000361820.3:c.1073A>G ENSP00000355155.3:p.Asp358Gly
NM_133445.2:c.1073A>G NP_597702.2:p.Asp358Gly
XM_011518211.1:c.1073A>G XP_011516513.1:p.Asp358Gly
XM_011518212.1:c.1073A>G XP_011516514.1:p.Asp358Gly
XR_929711.1:n.1160A>G
XM_011518211.2:c.1073A>G XP_011516513.1:p.Asp358Gly
NM_133445.3:c.1073A>G MANE Select NP_597702.2:p.Asp358Gly
Search 100 bp 5'
Search 100 bp 3'