Canonical Allele Identifier: CA2575085651

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13570038C>G , CM000674.2:g.13570038C>G	GRCh38
NC_000012.11:g.13722972C>G , CM000674.1:g.13722972C>G	GRCh37
NC_000012.10:g.13614239C>G	NCBI36
NG_031854.1:g.415051G>C
NG_031854.2:g.416975G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.2172-21G>C MANE Select	ENSP00000477455.1:n.2172-21G>C
ENST00000628166.2:n.432-21G>C
ENST00000637214.1:c.69+38565G>C	ENSP00000489997.1:n.69+38565G>C
ENST00000609686.3:c.2172-21G>C	ENSP00000477455.1:n.2172-21G>C
ENST00000628166.1:n.432-21G>C
NM_000834.3:c.2172-21G>C	NP_000825.2:n.2172-21G>C
XM_005253351.2:c.-43-21G>C	XP_005253408.1:n.-43-21G>C
XM_011520628.1:c.2172-21G>C	XP_011518930.1:n.2172-21G>C
XM_011520629.1:c.2172-21G>C	XP_011518931.1:n.2172-21G>C
XM_011520630.1:c.2172-21G>C	XP_011518932.1:n.2172-21G>C
NM_000834.4:c.2172-21G>C	NP_000825.2:n.2172-21G>C
XM_005253351.3:c.-43-21G>C	XP_005253408.1:n.-43-21G>C
XM_011520628.2:c.2172-21G>C	XP_011518930.1:n.2172-21G>C
XM_011520629.2:c.2172-21G>C	XP_011518931.1:n.2172-21G>C
XM_017019219.2:c.2172-21G>C	XP_016874708.1:n.2172-21G>C
NM_000834.5:c.2172-21G>C MANE Select	NP_000825.2:n.2172-21G>C