Canonical Allele Identifier: CA2794601234

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562214T>G , CM000674.2:g.13562214T>G	GRCh38
NC_000012.11:g.13715148T>G , CM000674.1:g.13715148T>G	GRCh37
NC_000012.10:g.13606415T>G	NCBI36
NG_031854.1:g.422875A>C
NG_031854.2:g.424799A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*569A>C MANE Select	ENSP00000477455.1:n.*569A>C
ENST00000636207.1:n.54+24A>C
ENST00000637214.1:c.69+46389A>C	ENSP00000489997.1:n.69+46389A>C
ENST00000609686.3:c.*569A>C	ENSP00000477455.1:n.*569A>C
NM_000834.3:c.*569A>C	NP_000825.2:n.*569A>C
XM_005253351.2:c.*569A>C	XP_005253408.1:n.*569A>C
XM_011520628.1:c.*569A>C	XP_011518930.1:n.*569A>C
XM_011520629.1:c.*569A>C	XP_011518931.1:n.*569A>C
XM_011520630.1:c.*569A>C	XP_011518932.1:n.*569A>C
NM_000834.4:c.*569A>C	NP_000825.2:n.*569A>C
XM_005253351.3:c.*569A>C	XP_005253408.1:n.*569A>C
XM_011520628.2:c.*569A>C	XP_011518930.1:n.*569A>C
XM_011520629.2:c.*569A>C	XP_011518931.1:n.*569A>C
XM_017019219.2:c.*569A>C	XP_016874708.1:n.*569A>C
NM_000834.5:c.*569A>C MANE Select	NP_000825.2:n.*569A>C