Canonical Allele Identifier: CA2017438749
Gene: GRIN2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13566444G= , CM000674.2:g.13566444G= GRCh38
NC_000012.11:g.13719378G= , CM000674.1:g.13719378G= GRCh37
NC_000012.10:g.13610645G= NCBI36
NG_031854.1:g.418645C=
NG_031854.2:g.420569C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000609686.4:c.2598+581C= MANE Select ENSP00000477455.1:n.2598+581C=
ENST00000637214.1:c.69+42159C= ENSP00000489997.1:n.69+42159C=
ENST00000609686.3:c.2598+581C= ENSP00000477455.1:n.2598+581C=
ENST00000628166.1:n.858+581C=
NM_000834.3:c.2598+581C= NP_000825.2:n.2598+581C=
XM_005253351.2:c.384+581C= XP_005253408.1:n.384+581C=
XM_011520628.1:c.2598+581C= XP_011518930.1:n.2598+581C=
XM_011520629.1:c.2598+581C= XP_011518931.1:n.2598+581C=
XM_011520630.1:c.2598+581C= XP_011518932.1:n.2598+581C=
NM_000834.4:c.2598+581C= NP_000825.2:n.2598+581C=
XM_005253351.3:c.384+581C= XP_005253408.1:n.384+581C=
XM_011520628.2:c.2598+581C= XP_011518930.1:n.2598+581C=
XM_011520629.2:c.2598+581C= XP_011518931.1:n.2598+581C=
XM_017019219.2:c.2598+581C= XP_016874708.1:n.2598+581C=
NM_000834.5:c.2598+581C= MANE Select NP_000825.2:n.2598+581C=