Canonical Allele Identifier: CA725899857

Gene: GRIN2A

Linked Data

• dbSNP Id: rs1425420731
• gnomAD v3: 16-9976633-T-C
• gnomAD v4: 16-9976633-T-C
• MyVariant Identifiers: chr16:g.10070490T>C (hg19) ; chr16:g.9976633T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9976633T>C , CM000678.2:g.9976633T>C	GRCh38
NC_000016.9:g.10070490T>C , CM000678.1:g.10070490T>C	GRCh37
NC_000016.8:g.9977991T>C	NCBI36
NG_011812.1:g.211122A>G
NG_011812.2:g.211122A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000330684.4:c.415-38082A>G MANE Select	ENSP00000332549.3:n.415-38082A>G
ENST00000637393.1:c.7-38082A>G	ENSP00000490232.1:n.7-38082A>G
ENST00000674742.1:c.-57-38082A>G	ENSP00000502200.1:n.-57-38082A>G
ENST00000675189.1:n.899-38082A>G
ENST00000675398.1:c.415-38082A>G	ENSP00000502752.1:n.415-38082A>G
ENST00000330684.3:c.415-38082A>G	ENSP00000332549.3:n.415-38082A>G
ENST00000396573.6:c.415-38082A>G	ENSP00000379818.2:n.415-38082A>G
ENST00000562109.5:c.415-38082A>G	ENSP00000454998.1:n.415-38082A>G
ENST00000566670.2:n.257-38082A>G
ENST00000566683.1:n.240+54692A>G
ENST00000568247.3:n.141-33337A>G
NM_000833.4:c.415-38082A>G	NP_000824.1:n.415-38082A>G
NM_001134407.2:c.415-38082A>G	NP_001127879.1:n.415-38082A>G
NM_001134408.2:c.415-38082A>G	NP_001127880.1:n.415-38082A>G
XM_011522456.1:c.256-38082A>G	XP_011520758.1:n.256-38082A>G
XM_011522458.1:c.-57-38082A>G	XP_011520760.1:n.-57-38082A>G
XM_011522459.1:c.-201-21933A>G	XP_011520761.1:n.-201-21933A>G
XM_011522460.1:c.-197-21937A>G	XP_011520762.1:n.-197-21937A>G
XM_011522461.1:c.415-38082A>G	XP_011520763.1:n.415-38082A>G
XM_011522458.3:c.-57-38082A>G	XP_011520760.1:n.-57-38082A>G
XM_011522461.3:c.415-38082A>G	XP_011520763.1:n.415-38082A>G
XM_017023172.1:c.571-38082A>G	XP_016878661.1:n.571-38082A>G
XM_017023173.1:c.571-38082A>G	XP_016878662.1:n.571-38082A>G
NM_001134407.3:c.415-38082A>G MANE Select	NP_001127879.1:n.415-38082A>G
NM_000833.5:c.415-38082A>G	NP_000824.1:n.415-38082A>G