Canonical Allele Identifier: CA466654029
Gene: GRIN3A HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.104449105G>C (hg19)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000361820.6:c.1077C>G MANE Select ENSP00000355155.3:p.Ser359=
ENST00000361820.3:c.1077C>G ENSP00000355155.3:p.Ser359=
NM_133445.2:c.1077C>G NP_597702.2:p.Ser359=
XM_011518211.1:c.1077C>G XP_011516513.1:p.Ser359=
XM_011518212.1:c.1077C>G XP_011516514.1:p.Ser359=
XR_929711.1:n.1164C>G
XM_011518211.2:c.1077C>G XP_011516513.1:p.Ser359=
NM_133445.3:c.1077C>G MANE Select NP_597702.2:p.Ser359=
Search 100 bp 5'
Search 100 bp 3'