Canonical Allele Identifier: CA374271699
Gene: GRIN3A HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.104449112C>A (hg19) chr9:g.101686830C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101686830C>A , CM000671.2:g.101686830C>A GRCh38
NC_000009.11:g.104449112C>A , CM000671.1:g.104449112C>A GRCh37
NC_000009.10:g.103488933C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.1070G>T MANE Select ENSP00000355155.3:p.Gly357Val
ENST00000361820.3:c.1070G>T ENSP00000355155.3:p.Gly357Val
NM_133445.2:c.1070G>T NP_597702.2:p.Gly357Val
XM_011518211.1:c.1070G>T XP_011516513.1:p.Gly357Val
XM_011518212.1:c.1070G>T XP_011516514.1:p.Gly357Val
XR_929711.1:n.1157G>T
XM_011518211.2:c.1070G>T XP_011516513.1:p.Gly357Val
NM_133445.3:c.1070G>T MANE Select NP_597702.2:p.Gly357Val
Search 100 bp 5'
Search 100 bp 3'