Canonical Allele Identifier: CA2617751740

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13615678-GAAACAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615686_13615691del , CM000674.2:g.13615686_13615691del	GRCh38
NC_000012.11:g.13768620_13768625del , CM000674.1:g.13768620_13768625del	GRCh37
NC_000012.10:g.13659887_13659892del	NCBI36
NG_031854.1:g.369405_369410del
NG_031854.2:g.371329_371334del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1329-20_1329-15del MANE Select	ENSP00000477455.1:n.1329-20_1329-15del
ENST00000630791.2:c.1329-20_1329-15del	ENSP00000486677.2:n.1329-20_1329-15del
ENST00000609686.3:c.1329-20_1329-15del	ENSP00000477455.1:n.1329-20_1329-15del
NM_000834.3:c.1329-20_1329-15del	NP_000825.2:n.1329-20_1329-15del
XM_011520628.1:c.1329-20_1329-15del	XP_011518930.1:n.1329-20_1329-15del
XM_011520629.1:c.1329-20_1329-15del	XP_011518931.1:n.1329-20_1329-15del
XM_011520630.1:c.1329-20_1329-15del	XP_011518932.1:n.1329-20_1329-15del
XR_931372.1:n.307+460_307+465del
XR_931373.1:n.447+460_447+465del
XR_931374.1:n.246+460_246+465del
NM_000834.4:c.1329-20_1329-15del	NP_000825.2:n.1329-20_1329-15del
XM_011520628.2:c.1329-20_1329-15del	XP_011518930.1:n.1329-20_1329-15del
XM_011520629.2:c.1329-20_1329-15del	XP_011518931.1:n.1329-20_1329-15del
XM_017019219.2:c.1329-20_1329-15del	XP_016874708.1:n.1329-20_1329-15del
XR_001749013.1:n.728+460_728+465del
XR_931372.2:n.444+460_444+465del
XR_931373.2:n.586+460_586+465del
NM_000834.5:c.1329-20_1329-15del MANE Select	NP_000825.2:n.1329-20_1329-15del