Canonical Allele Identifier: CA717851476

Gene: GRIN2A

Linked Data

• dbSNP Id: rs1316959780
• gnomAD v3: 16-10180505-C-A
• gnomAD v4: 16-10180505-C-A
• MyVariant Identifiers: chr16:g.10274362C>A (hg19) ; chr16:g.10180505C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180505C>A , CM000678.2:g.10180505C>A	GRCh38
NC_000016.9:g.10274362C>A , CM000678.1:g.10274362C>A	GRCh37
NC_000016.8:g.10181863C>A	NCBI36
NG_011812.1:g.7250G>T
NG_011812.2:g.7250G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.-18-76G>T MANE Select	ENSP00000332549.3:n.-18-76G>T
ENST00000636406.1:c.-18-76G>T	ENSP00000490676.1:n.-18-76G>T
ENST00000637188.1:c.-18-76G>T	ENSP00000489946.1:n.-18-76G>T
ENST00000675189.1:n.467-76G>T
ENST00000675398.1:c.-18-76G>T	ENSP00000502752.1:n.-18-76G>T
ENST00000676032.1:n.416-76G>T
ENST00000330684.3:c.-18-76G>T	ENSP00000332549.3:n.-18-76G>T
ENST00000396573.6:c.-18-76G>T	ENSP00000379818.2:n.-18-76G>T
ENST00000562109.5:c.-18-76G>T	ENSP00000454998.1:n.-18-76G>T
ENST00000566665.1:n.384-76G>T
NM_000833.4:c.-18-76G>T	NP_000824.1:n.-18-76G>T
NM_001134407.2:c.-18-76G>T	NP_001127879.1:n.-18-76G>T
NM_001134408.2:c.-18-76G>T	NP_001127880.1:n.-18-76G>T
XM_011522461.1:c.-18-76G>T	XP_011520763.1:n.-18-76G>T
XM_011522461.3:c.-18-76G>T	XP_011520763.1:n.-18-76G>T
XM_017023172.1:c.63G>T	XP_016878661.1:p.Gln21His
XM_017023173.1:c.63G>T	XP_016878662.1:p.Gln21His
NM_001134407.3:c.-18-76G>T MANE Select	NP_001127879.1:n.-18-76G>T
NM_000833.5:c.-18-76G>T	NP_000824.1:n.-18-76G>T