Canonical Allele Identifier: CA603450352

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1283249299
• gnomAD v2: 12-13770247-T-C
• gnomAD v3: 12-13617313-T-C
• gnomAD v4: 12-13617313-T-C
• MyVariant Identifiers: chr12:g.13770247T>C (hg19) ; chr12:g.13617313T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13617313T>C , CM000674.2:g.13617313T>C	GRCh38
NC_000012.11:g.13770247T>C , CM000674.1:g.13770247T>C	GRCh37
NC_000012.10:g.13661514T>C	NCBI36
NG_031854.1:g.367776A>G
NG_031854.2:g.369700A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.1126-656A>G MANE Select	ENSP00000477455.1:n.1126-656A>G
ENST00000630791.2:c.1126-656A>G	ENSP00000486677.2:n.1126-656A>G
ENST00000609686.3:c.1126-656A>G	ENSP00000477455.1:n.1126-656A>G
NM_000834.3:c.1126-656A>G	NP_000825.2:n.1126-656A>G
XM_011520628.1:c.1126-656A>G	XP_011518930.1:n.1126-656A>G
XM_011520629.1:c.1126-656A>G	XP_011518931.1:n.1126-656A>G
XM_011520630.1:c.1126-656A>G	XP_011518932.1:n.1126-656A>G
XR_931372.1:n.307+2087T>C
XR_931373.1:n.447+2087T>C
XR_931374.1:n.246+2087T>C
NM_000834.4:c.1126-656A>G	NP_000825.2:n.1126-656A>G
XM_011520628.2:c.1126-656A>G	XP_011518930.1:n.1126-656A>G
XM_011520629.2:c.1126-656A>G	XP_011518931.1:n.1126-656A>G
XM_017019219.2:c.1126-656A>G	XP_016874708.1:n.1126-656A>G
XR_001749013.1:n.728+2087T>C
XR_931372.2:n.444+2087T>C
XR_931373.2:n.586+2087T>C
NM_000834.5:c.1126-656A>G MANE Select	NP_000825.2:n.1126-656A>G