Canonical Allele Identifier: CA2978650746

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562292C>G , CM000674.2:g.13562292C>G	GRCh38
NC_000012.11:g.13715226C>G , CM000674.1:g.13715226C>G	GRCh37
NC_000012.10:g.13606493C>G	NCBI36
NG_031854.1:g.422797G>C
NG_031854.2:g.424721G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*491G>C MANE Select	ENSP00000477455.1:n.*491G>C
ENST00000637214.1:c.69+46311G>C	ENSP00000489997.1:n.69+46311G>C
ENST00000609686.3:c.*491G>C	ENSP00000477455.1:n.*491G>C
NM_000834.3:c.*491G>C	NP_000825.2:n.*491G>C
XM_005253351.2:c.*491G>C	XP_005253408.1:n.*491G>C
XM_011520628.1:c.*491G>C	XP_011518930.1:n.*491G>C
XM_011520629.1:c.*491G>C	XP_011518931.1:n.*491G>C
XM_011520630.1:c.*491G>C	XP_011518932.1:n.*491G>C
NM_000834.4:c.*491G>C	NP_000825.2:n.*491G>C
XM_005253351.3:c.*491G>C	XP_005253408.1:n.*491G>C
XM_011520628.2:c.*491G>C	XP_011518930.1:n.*491G>C
XM_011520629.2:c.*491G>C	XP_011518931.1:n.*491G>C
XM_017019219.2:c.*491G>C	XP_016874708.1:n.*491G>C
NM_000834.5:c.*491G>C MANE Select	NP_000825.2:n.*491G>C