Canonical Allele Identifier: CA383996074

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1407933201
• gnomAD v2: 12-13720011-C-T
• MyVariant Identifiers: chr12:g.13720011C>T (hg19) ; chr12:g.13567077C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13567077C>T , CM000674.2:g.13567077C>T	GRCh38
NC_000012.11:g.13720011C>T , CM000674.1:g.13720011C>T	GRCh37
NC_000012.10:g.13611278C>T	NCBI36
NG_031854.1:g.418012G>A
NG_031854.2:g.419936G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.2546G>A MANE Select	ENSP00000477455.1:p.Cys849Tyr
ENST00000637214.1:c.69+41526G>A	ENSP00000489997.1:n.69+41526G>A
ENST00000609686.3:c.2546G>A	ENSP00000477455.1:p.Cys849Tyr
ENST00000628166.1:n.806G>A
NM_000834.3:c.2546G>A	NP_000825.2:p.Cys849Tyr
XM_005253351.2:c.332G>A	XP_005253408.1:p.Cys111Tyr
XM_011520628.1:c.2546G>A	XP_011518930.1:p.Cys849Tyr
XM_011520629.1:c.2546G>A	XP_011518931.1:p.Cys849Tyr
XM_011520630.1:c.2546G>A	XP_011518932.1:p.Cys849Tyr
NM_000834.4:c.2546G>A	NP_000825.2:p.Cys849Tyr
XM_005253351.3:c.332G>A	XP_005253408.1:p.Cys111Tyr
XM_011520628.2:c.2546G>A	XP_011518930.1:p.Cys849Tyr
XM_011520629.2:c.2546G>A	XP_011518931.1:p.Cys849Tyr
XM_017019219.2:c.2546G>A	XP_016874708.1:p.Cys849Tyr
NM_000834.5:c.2546G>A MANE Select	NP_000825.2:p.Cys849Tyr