Canonical Allele Identifier: CA466654038
Gene: GRIN3A HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.104449111T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101686829T>G , CM000671.2:g.101686829T>G GRCh38
NC_000009.11:g.104449111T>G , CM000671.1:g.104449111T>G GRCh37
NC_000009.10:g.103488932T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.1071A>C MANE Select ENSP00000355155.3:p.Gly357=
ENST00000361820.3:c.1071A>C ENSP00000355155.3:p.Gly357=
NM_133445.2:c.1071A>C NP_597702.2:p.Gly357=
XM_011518211.1:c.1071A>C XP_011516513.1:p.Gly357=
XM_011518212.1:c.1071A>C XP_011516514.1:p.Gly357=
XR_929711.1:n.1158A>C
XM_011518211.2:c.1071A>C XP_011516513.1:p.Gly357=
NM_133445.3:c.1071A>C MANE Select NP_597702.2:p.Gly357=
Search 100 bp 5'
Search 100 bp 3'