Canonical Allele Identifier: CA466470751
Gene: GRIN3A HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.104449000C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101686718C>T , CM000671.2:g.101686718C>T GRCh38
NC_000009.11:g.104449000C>T , CM000671.1:g.104449000C>T GRCh37
NC_000009.10:g.103488821C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361820.6:c.1182G>A MANE Select ENSP00000355155.3:p.Glu394=
ENST00000361820.3:c.1182G>A ENSP00000355155.3:p.Glu394=
NM_133445.2:c.1182G>A NP_597702.2:p.Glu394=
XM_011518211.1:c.1182G>A XP_011516513.1:p.Glu394=
XM_011518212.1:c.1182G>A XP_011516514.1:p.Glu394=
XR_929711.1:n.1269G>A
XM_011518211.2:c.1182G>A XP_011516513.1:p.Glu394=
NM_133445.3:c.1182G>A MANE Select NP_597702.2:p.Glu394=
Search 100 bp 5'
Search 100 bp 3'