Canonical Allele Identifier: CA2017437738

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562563_13562564delinsCG , CM000674.2:g.13562563_13562564delinsCG	GRCh38
NC_000012.11:g.13715497_13715498delinsCG , CM000674.1:g.13715497_13715498delinsCG	GRCh37
NC_000012.10:g.13606764_13606765delinsCG	NCBI36
NG_031854.1:g.422525_422526delinsCG
NG_031854.2:g.424449_424450delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*219_*220delinsCG MANE Select	ENSP00000477455.1:n.*219_*220delinsCG
ENST00000637214.1:c.69+46039_69+46040delinsCG	ENSP00000489997.1:n.69+46039_69+46040delinsCG
ENST00000609686.3:c.*219_*220delinsCG	ENSP00000477455.1:n.*219_*220delinsCG
NM_000834.3:c.*219_*220delinsCG	NP_000825.2:n.*219_*220delinsCG
XM_005253351.2:c.*219_*220delinsCG	XP_005253408.1:n.*219_*220delinsCG
XM_011520628.1:c.*219_*220delinsCG	XP_011518930.1:n.*219_*220delinsCG
XM_011520629.1:c.*219_*220delinsCG	XP_011518931.1:n.*219_*220delinsCG
XM_011520630.1:c.*219_*220delinsCG	XP_011518932.1:n.*219_*220delinsCG
NM_000834.4:c.*219_*220delinsCG	NP_000825.2:n.*219_*220delinsCG
XM_005253351.3:c.*219_*220delinsCG	XP_005253408.1:n.*219_*220delinsCG
XM_011520628.2:c.*219_*220delinsCG	XP_011518930.1:n.*219_*220delinsCG
XM_011520629.2:c.*219_*220delinsCG	XP_011518931.1:n.*219_*220delinsCG
XM_017019219.2:c.*219_*220delinsCG	XP_016874708.1:n.*219_*220delinsCG
NM_000834.5:c.*219_*220delinsCG MANE Select	NP_000825.2:n.*219_*220delinsCG