Canonical Allele Identifier: CA2017510017

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1950484513

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13719016G>T , CM000674.2:g.13719016G>T	GRCh38
NC_000012.11:g.13871950G>T , CM000674.1:g.13871950G>T	GRCh37
NC_000012.10:g.13763217G>T	NCBI36
NG_031854.1:g.266073C>A
NG_031854.2:g.267997C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.1010+34301C>A MANE Select	ENSP00000477455.1:n.1010+34301C>A
ENST00000630791.2:c.1010+34301C>A	ENSP00000486677.2:n.1010+34301C>A
ENST00000609686.3:c.1010+34301C>A	ENSP00000477455.1:n.1010+34301C>A
NM_000834.3:c.1010+34301C>A	NP_000825.2:n.1010+34301C>A
XM_011520628.1:c.1010+34301C>A	XP_011518930.1:n.1010+34301C>A
XM_011520629.1:c.1010+34301C>A	XP_011518931.1:n.1010+34301C>A
XM_011520630.1:c.1010+34301C>A	XP_011518932.1:n.1010+34301C>A
NM_000834.4:c.1010+34301C>A	NP_000825.2:n.1010+34301C>A
XM_011520628.2:c.1010+34301C>A	XP_011518930.1:n.1010+34301C>A
XM_011520629.2:c.1010+34301C>A	XP_011518931.1:n.1010+34301C>A
XM_017019219.2:c.1010+34301C>A	XP_016874708.1:n.1010+34301C>A
NM_000834.5:c.1010+34301C>A MANE Select	NP_000825.2:n.1010+34301C>A