Canonical Allele Identifier: CA2017463222

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1949424728

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615432_13615438del , CM000674.2:g.13615432_13615438del	GRCh38
NC_000012.11:g.13768366_13768372del , CM000674.1:g.13768366_13768372del	GRCh37
NC_000012.10:g.13659633_13659639del	NCBI36
NG_031854.1:g.369651_369657del
NG_031854.2:g.371575_371581del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1500+55_1500+61del MANE Select	ENSP00000477455.1:n.1500+55_1500+61del
ENST00000609686.3:c.1500+55_1500+61del	ENSP00000477455.1:n.1500+55_1500+61del
NM_000834.3:c.1500+55_1500+61del	NP_000825.2:n.1500+55_1500+61del
XM_011520628.1:c.1500+55_1500+61del	XP_011518930.1:n.1500+55_1500+61del
XM_011520629.1:c.1500+55_1500+61del	XP_011518931.1:n.1500+55_1500+61del
XM_011520630.1:c.1500+55_1500+61del	XP_011518932.1:n.1500+55_1500+61del
XR_931372.1:n.307+206_307+212del
XR_931373.1:n.447+206_447+212del
XR_931374.1:n.246+206_246+212del
NM_000834.4:c.1500+55_1500+61del	NP_000825.2:n.1500+55_1500+61del
XM_011520628.2:c.1500+55_1500+61del	XP_011518930.1:n.1500+55_1500+61del
XM_011520629.2:c.1500+55_1500+61del	XP_011518931.1:n.1500+55_1500+61del
XM_017019219.2:c.1500+55_1500+61del	XP_016874708.1:n.1500+55_1500+61del
XR_001749013.1:n.728+206_728+212del
XR_931372.2:n.444+206_444+212del
XR_931373.2:n.586+206_586+212del
NM_000834.5:c.1500+55_1500+61del MANE Select	NP_000825.2:n.1500+55_1500+61del