Canonical Allele Identifier: CA2017463099

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1949422865

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615333del , CM000674.2:g.13615333del	GRCh38
NC_000012.11:g.13768267del , CM000674.1:g.13768267del	GRCh37
NC_000012.10:g.13659534del	NCBI36
NG_031854.1:g.369756del
NG_031854.2:g.371680del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1501-66del MANE Select	ENSP00000477455.1:n.1501-66del
ENST00000609686.3:c.1501-66del	ENSP00000477455.1:n.1501-66del
NM_000834.3:c.1501-66del	NP_000825.2:n.1501-66del
XM_011520628.1:c.1501-66del	XP_011518930.1:n.1501-66del
XM_011520629.1:c.1501-66del	XP_011518931.1:n.1501-66del
XM_011520630.1:c.1501-66del	XP_011518932.1:n.1501-66del
XR_931372.1:n.307+107del
XR_931373.1:n.447+107del
XR_931374.1:n.246+107del
NM_000834.4:c.1501-66del	NP_000825.2:n.1501-66del
XM_011520628.2:c.1501-66del	XP_011518930.1:n.1501-66del
XM_011520629.2:c.1501-66del	XP_011518931.1:n.1501-66del
XM_017019219.2:c.1501-66del	XP_016874708.1:n.1501-66del
XR_001749013.1:n.728+107del
XR_931372.2:n.444+107del
XR_931373.2:n.586+107del
NM_000834.5:c.1501-66del MANE Select	NP_000825.2:n.1501-66del