Canonical Allele Identifier: CA466654028
Gene: GRIN3A HGNC NCBI

Linked Data

gnomAD v4: 9-101686823-G-A
COSMIC: COSM1239025
MyVariant Identifiers: chr9:g.104449105G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101686823G>A , CM000671.2:g.101686823G>A GRCh38
NC_000009.11:g.104449105G>A , CM000671.1:g.104449105G>A GRCh37
NC_000009.10:g.103488926G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.1077C>T MANE Select ENSP00000355155.3:p.Ser359=
ENST00000361820.3:c.1077C>T ENSP00000355155.3:p.Ser359=
NM_133445.2:c.1077C>T NP_597702.2:p.Ser359=
XM_011518211.1:c.1077C>T XP_011516513.1:p.Ser359=
XM_011518212.1:c.1077C>T XP_011516514.1:p.Ser359=
XR_929711.1:n.1164C>T
XM_011518211.2:c.1077C>T XP_011516513.1:p.Ser359=
NM_133445.3:c.1077C>T MANE Select NP_597702.2:p.Ser359=
Search 100 bp 5'
Search 100 bp 3'