Canonical Allele Identifier: CA384051752

Gene: GRIN2B

Linked Data

• MyVariant Identifiers: chr12:g.13768087A>T (hg19) ; chr12:g.13615153A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615153A>T , CM000674.2:g.13615153A>T	GRCh38
NC_000012.11:g.13768087A>T , CM000674.1:g.13768087A>T	GRCh37
NC_000012.10:g.13659354A>T	NCBI36
NG_031854.1:g.369936T>A
NG_031854.2:g.371860T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.1615T>A MANE Select	ENSP00000477455.1:p.Ser539Thr
ENST00000609686.3:c.1615T>A	ENSP00000477455.1:p.Ser539Thr
NM_000834.3:c.1615T>A	NP_000825.2:p.Ser539Thr
XM_011520628.1:c.1615T>A	XP_011518930.1:p.Ser539Thr
XM_011520629.1:c.1615T>A	XP_011518931.1:p.Ser539Thr
XM_011520630.1:c.1615T>A	XP_011518932.1:p.Ser539Thr
XR_931372.1:n.234A>T
XR_931373.1:n.374A>T
XR_931374.1:n.173A>T
NM_000834.4:c.1615T>A	NP_000825.2:p.Ser539Thr
XM_011520628.2:c.1615T>A	XP_011518930.1:p.Ser539Thr
XM_011520629.2:c.1615T>A	XP_011518931.1:p.Ser539Thr
XM_017019219.2:c.1615T>A	XP_016874708.1:p.Ser539Thr
XR_001749013.1:n.655A>T
XR_931372.2:n.371A>T
XR_931373.2:n.513A>T
NM_000834.5:c.1615T>A MANE Select	NP_000825.2:p.Ser539Thr