Canonical Allele Identifier: CA233131023

Gene: GRIN2B

Identifiers and link-outs to other resources

• dbSNP Id: rs1805501
• gnomAD: 12:13714059 A / G
• MyVariant Identifiers: chr12:g.13714059A>G (hg19) ; chr12:g.13561125A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13561125A>G , CM000674.2:g.13561125A>G	GRCh38
NC_000012.11:g.13714059A>G , CM000674.1:g.13714059A>G	GRCh37
NC_000012.10:g.13605326A>G	NCBI36
NG_031854.1:g.423964T>C
NG_031854.2:g.425888T>C

Transcript Alleles

HGVS	Amino-acid change
XM_005253351.2:c.*1658T>C	XP_005253408.1:p.=
XM_011520628.1:c.*1658T>C	XP_011518930.1:p.=
XM_011520629.1:c.*1658T>C	XP_011518931.1:p.=
XM_011520630.1:c.*1658T>C	XP_011518932.1:p.=
NM_000834.4:c.*1658T>C VV	NP_000825.2:p.=
XM_005253351.3:c.*1658T>C	XP_005253408.1:p.=
XM_011520628.2:c.*1658T>C	XP_011518930.1:p.=
XM_011520629.2:c.*1658T>C	XP_011518931.1:p.=
XM_017019219.2:c.*1658T>C	XP_016874708.1:p.=
NM_000834.5:c.*1658T>C VV MANE Preferred	NP_000825.2:p.=
ENST00000609686.3:c.*1658T>C	ENSP00000477455.1:p.=