Canonical Allele Identifier: CA2580085173

Gene: GRIN2B

Linked Data

• ClinVar Variation Id: 2025942
• ClinVar RCV Id: RCV002858239

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615105A>G , CM000674.2:g.13615105A>G	GRCh38
NC_000012.11:g.13768039A>G , CM000674.1:g.13768039A>G	GRCh37
NC_000012.10:g.13659306A>G	NCBI36
NG_031854.1:g.369984T>C
NG_031854.2:g.371908T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1654+9T>C MANE Select	ENSP00000477455.1:n.1654+9T>C
ENST00000609686.3:c.1654+9T>C	ENSP00000477455.1:n.1654+9T>C
NM_000834.3:c.1654+9T>C	NP_000825.2:n.1654+9T>C
XM_011520628.1:c.1654+9T>C	XP_011518930.1:n.1654+9T>C
XM_011520629.1:c.1654+9T>C	XP_011518931.1:n.1654+9T>C
XM_011520630.1:c.1654+9T>C	XP_011518932.1:n.1654+9T>C
XR_931372.1:n.186A>G
XR_931373.1:n.326A>G
XR_931374.1:n.125A>G
NM_000834.4:c.1654+9T>C	NP_000825.2:n.1654+9T>C
XM_011520628.2:c.1654+9T>C	XP_011518930.1:n.1654+9T>C
XM_011520629.2:c.1654+9T>C	XP_011518931.1:n.1654+9T>C
XM_017019219.2:c.1654+9T>C	XP_016874708.1:n.1654+9T>C
XR_001749013.1:n.607A>G
XR_931372.2:n.323A>G
XR_931373.2:n.465A>G
NM_000834.5:c.1654+9T>C MANE Select	NP_000825.2:n.1654+9T>C