Canonical Allele Identifier: CA374271664
Gene: GRIN3A HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.104449106G>T (hg19) chr9:g.101686824G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101686824G>T , CM000671.2:g.101686824G>T GRCh38
NC_000009.11:g.104449106G>T , CM000671.1:g.104449106G>T GRCh37
NC_000009.10:g.103488927G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.1076C>A MANE Select ENSP00000355155.3:p.Ser359Tyr
ENST00000361820.3:c.1076C>A ENSP00000355155.3:p.Ser359Tyr
NM_133445.2:c.1076C>A NP_597702.2:p.Ser359Tyr
XM_011518211.1:c.1076C>A XP_011516513.1:p.Ser359Tyr
XM_011518212.1:c.1076C>A XP_011516514.1:p.Ser359Tyr
XR_929711.1:n.1163C>A
XM_011518211.2:c.1076C>A XP_011516513.1:p.Ser359Tyr
NM_133445.3:c.1076C>A MANE Select NP_597702.2:p.Ser359Tyr
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