Canonical Allele Identifier: CA2017463454
Gene: GRIN2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13615630T= , CM000674.2:g.13615630T= GRCh38
NC_000012.11:g.13768564T= , CM000674.1:g.13768564T= GRCh37
NC_000012.10:g.13659831T= NCBI36
NG_031854.1:g.369459A=
NG_031854.2:g.371383A=

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.1363A= MANE Select ENSP00000477455.1:p.Lys455=
ENST00000630791.2:c.1363A= ENSP00000486677.2:p.Lys455=
ENST00000609686.3:c.1363A= ENSP00000477455.1:p.Lys455=
NM_000834.3:c.1363A= NP_000825.2:p.Lys455=
XM_011520628.1:c.1363A= XP_011518930.1:p.Lys455=
XM_011520629.1:c.1363A= XP_011518931.1:p.Lys455=
XM_011520630.1:c.1363A= XP_011518932.1:p.Lys455=
XR_931372.1:n.307+404T=
XR_931373.1:n.447+404T=
XR_931374.1:n.246+404T=
NM_000834.4:c.1363A= NP_000825.2:p.Lys455=
XM_011520628.2:c.1363A= XP_011518930.1:p.Lys455=
XM_011520629.2:c.1363A= XP_011518931.1:p.Lys455=
XM_017019219.2:c.1363A= XP_016874708.1:p.Lys455=
XR_001749013.1:n.728+404T=
XR_931372.2:n.444+404T=
XR_931373.2:n.586+404T=
NM_000834.5:c.1363A= MANE Select NP_000825.2:p.Lys455=