Canonical Allele Identifier: CA374271648
Gene: GRIN3A HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.104449103T>G (hg19) chr9:g.101686821T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101686821T>G , CM000671.2:g.101686821T>G GRCh38
NC_000009.11:g.104449103T>G , CM000671.1:g.104449103T>G GRCh37
NC_000009.10:g.103488924T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.1079A>C MANE Select ENSP00000355155.3:p.Gln360Pro
ENST00000361820.3:c.1079A>C ENSP00000355155.3:p.Gln360Pro
NM_133445.2:c.1079A>C NP_597702.2:p.Gln360Pro
XM_011518211.1:c.1079A>C XP_011516513.1:p.Gln360Pro
XM_011518212.1:c.1079A>C XP_011516514.1:p.Gln360Pro
XR_929711.1:n.1166A>C
XM_011518211.2:c.1079A>C XP_011516513.1:p.Gln360Pro
NM_133445.3:c.1079A>C MANE Select NP_597702.2:p.Gln360Pro
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