Canonical Allele Identifier: CA383990728

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1591606676
• MyVariant Identifiers: chr12:g.13717032T>G (hg19) ; chr12:g.13564098T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13564098T>G , CM000674.2:g.13564098T>G	GRCh38
NC_000012.11:g.13717032T>G , CM000674.1:g.13717032T>G	GRCh37
NC_000012.10:g.13608299T>G	NCBI36
NG_031854.1:g.420991A>C
NG_031854.2:g.422915A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.3140A>C MANE Select	ENSP00000477455.1:p.Asp1047Ala
ENST00000637214.1:c.69+44505A>C	ENSP00000489997.1:n.69+44505A>C
ENST00000609686.3:c.3140A>C	ENSP00000477455.1:p.Asp1047Ala
ENST00000628166.1:n.1400A>C
NM_000834.3:c.3140A>C	NP_000825.2:p.Asp1047Ala
XM_005253351.2:c.926A>C	XP_005253408.1:p.Asp309Ala
XM_011520628.1:c.3140A>C	XP_011518930.1:p.Asp1047Ala
XM_011520629.1:c.3140A>C	XP_011518931.1:p.Asp1047Ala
XM_011520630.1:c.3140A>C	XP_011518932.1:p.Asp1047Ala
NM_000834.4:c.3140A>C	NP_000825.2:p.Asp1047Ala
XM_005253351.3:c.926A>C	XP_005253408.1:p.Asp309Ala
XM_011520628.2:c.3140A>C	XP_011518930.1:p.Asp1047Ala
XM_011520629.2:c.3140A>C	XP_011518931.1:p.Asp1047Ala
XM_017019219.2:c.3140A>C	XP_016874708.1:p.Asp1047Ala
NM_000834.5:c.3140A>C MANE Select	NP_000825.2:p.Asp1047Ala