Canonical Allele Identifier: CA16620319
Gene: GRIN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 423850
ClinVar RCV Id: RCV000484465 RCV001823142
dbSNP Id: rs1064796658
MyVariant Identifiers: chr16:g.9858227G>T (hg19) chr16:g.9764370G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9764370G>T , CM000678.2:g.9764370G>T GRCh38
NC_000016.9:g.9858227G>T , CM000678.1:g.9858227G>T GRCh37
NC_000016.8:g.9765728G>T NCBI36
NG_011812.1:g.423385C>A
NG_011812.2:g.423385C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000330684.4:c.3174C>A MANE Select ENSP00000332549.3:p.His1058Gln
ENST00000535259.6:c.2703C>A ENSP00000441572.3:p.His901Gln
ENST00000636273.2:n.2767C>A
ENST00000674742.1:c.2703C>A ENSP00000502200.1:p.His901Gln
ENST00000675398.1:c.*544C>A ENSP00000502752.1:n.*544C>A
ENST00000330684.3:c.3174C>A ENSP00000332549.3:p.His1058Gln
ENST00000396573.6:c.3174C>A ENSP00000379818.2:p.His1058Gln
ENST00000396575.6:c.2763C>A ENSP00000379820.3:p.His921Gln
ENST00000461292.3:n.2813C>A
ENST00000535259.5:c.2763C>A ENSP00000441572.2:p.His921Gln
ENST00000562109.5:c.3174C>A ENSP00000454998.1:p.His1058Gln
NM_000833.4:c.3174C>A NP_000824.1:p.His1058Gln
NM_001134407.2:c.3174C>A NP_001127879.1:p.His1058Gln
NM_001134408.2:c.3174C>A NP_001127880.1:p.His1058Gln
XM_011522456.1:c.3015C>A XP_011520758.1:p.His1005Gln
XM_011522457.1:c.2916C>A XP_011520759.1:p.His972Gln
XM_011522458.1:c.2703C>A XP_011520760.1:p.His901Gln
XM_011522459.1:c.2703C>A XP_011520761.1:p.His901Gln
XM_011522460.1:c.2703C>A XP_011520762.1:p.His901Gln
XM_011522461.1:c.3174C>A XP_011520763.1:p.His1058Gln
XM_011522458.3:c.2703C>A XP_011520760.1:p.His901Gln
XM_011522461.3:c.3174C>A XP_011520763.1:p.His1058Gln
XM_017023172.1:c.3330C>A XP_016878661.1:p.His1110Gln
XM_017023173.1:c.3330C>A XP_016878662.1:p.His1110Gln
NM_001134407.3:c.3174C>A MANE Select NP_001127879.1:p.His1058Gln
NM_000833.5:c.3174C>A NP_000824.1:p.His1058Gln
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