Canonical Allele Identifier: CA374271651
Gene: GRIN3A HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.104449104G>A (hg19) chr9:g.101686822G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101686822G>A , CM000671.2:g.101686822G>A GRCh38
NC_000009.11:g.104449104G>A , CM000671.1:g.104449104G>A GRCh37
NC_000009.10:g.103488925G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.1078C>T MANE Select ENSP00000355155.3:p.Gln360Ter
ENST00000361820.3:c.1078C>T ENSP00000355155.3:p.Gln360Ter
NM_133445.2:c.1078C>T NP_597702.2:p.Gln360Ter
XM_011518211.1:c.1078C>T XP_011516513.1:p.Gln360Ter
XM_011518212.1:c.1078C>T XP_011516514.1:p.Gln360Ter
XR_929711.1:n.1165C>T
XM_011518211.2:c.1078C>T XP_011516513.1:p.Gln360Ter
NM_133445.3:c.1078C>T MANE Select NP_597702.2:p.Gln360Ter
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