Canonical Allele Identifier: CA384054370

Gene: GRIN2B

Linked Data

• MyVariant Identifiers: chr12:g.13906702G>T (hg19) ; chr12:g.13753768G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13753768G>T , CM000674.2:g.13753768G>T	GRCh38
NC_000012.11:g.13906702G>T , CM000674.1:g.13906702G>T	GRCh37
NC_000012.10:g.13797969G>T	NCBI36
NG_031854.1:g.231321C>A
NG_031854.2:g.233245C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.559C>A MANE Select	ENSP00000477455.1:p.Arg187Ser
ENST00000630791.2:c.559C>A	ENSP00000486677.2:p.Arg187Ser
ENST00000609686.3:c.559C>A	ENSP00000477455.1:p.Arg187Ser
NM_000834.3:c.559C>A	NP_000825.2:p.Arg187Ser
XM_011520628.1:c.559C>A	XP_011518930.1:p.Arg187Ser
XM_011520629.1:c.559C>A	XP_011518931.1:p.Arg187Ser
XM_011520630.1:c.559C>A	XP_011518932.1:p.Arg187Ser
NM_000834.4:c.559C>A	NP_000825.2:p.Arg187Ser
XM_011520628.2:c.559C>A	XP_011518930.1:p.Arg187Ser
XM_011520629.2:c.559C>A	XP_011518931.1:p.Arg187Ser
XM_017019219.2:c.559C>A	XP_016874708.1:p.Arg187Ser
NM_000834.5:c.559C>A MANE Select	NP_000825.2:p.Arg187Ser