Canonical Allele Identifier: CA374271672
Gene: GRIN3A HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.104449107A>T (hg19) chr9:g.101686825A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101686825A>T , CM000671.2:g.101686825A>T GRCh38
NC_000009.11:g.104449107A>T , CM000671.1:g.104449107A>T GRCh37
NC_000009.10:g.103488928A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.1075T>A MANE Select ENSP00000355155.3:p.Ser359Thr
ENST00000361820.3:c.1075T>A ENSP00000355155.3:p.Ser359Thr
NM_133445.2:c.1075T>A NP_597702.2:p.Ser359Thr
XM_011518211.1:c.1075T>A XP_011516513.1:p.Ser359Thr
XM_011518212.1:c.1075T>A XP_011516514.1:p.Ser359Thr
XR_929711.1:n.1162T>A
XM_011518211.2:c.1075T>A XP_011516513.1:p.Ser359Thr
NM_133445.3:c.1075T>A MANE Select NP_597702.2:p.Ser359Thr
Search 100 bp 5'
Search 100 bp 3'