Canonical Allele Identifier: CA2017447561
Gene: GRIN2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13608564A= , CM000674.2:g.13608564A= GRCh38
NC_000012.11:g.13761498A= , CM000674.1:g.13761498A= GRCh37
NC_000012.10:g.13652765A= NCBI36
NG_031854.1:g.376525T=
NG_031854.2:g.378449T=

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.2010+39T= MANE Select ENSP00000477455.1:n.2010+39T=
ENST00000628166.2:n.270+39T=
ENST00000637214.1:c.69+39T= ENSP00000489997.1:n.69+39T=
ENST00000609686.3:c.2010+39T= ENSP00000477455.1:n.2010+39T=
ENST00000628166.1:n.270+39T=
NM_000834.3:c.2010+39T= NP_000825.2:n.2010+39T=
XM_005253351.2:c.-44+39T= XP_005253408.1:n.-44+39T=
XM_011520628.1:c.2010+39T= XP_011518930.1:n.2010+39T=
XM_011520629.1:c.2010+39T= XP_011518931.1:n.2010+39T=
XM_011520630.1:c.2010+39T= XP_011518932.1:n.2010+39T=
XR_931372.1:n.179-6534A=
XR_931373.1:n.179-54A=
NM_000834.4:c.2010+39T= NP_000825.2:n.2010+39T=
XM_005253351.3:c.-44+39T= XP_005253408.1:n.-44+39T=
XM_011520628.2:c.2010+39T= XP_011518930.1:n.2010+39T=
XM_011520629.2:c.2010+39T= XP_011518931.1:n.2010+39T=
XM_017019219.2:c.2010+39T= XP_016874708.1:n.2010+39T=
XR_001749013.1:n.318-54A=
XR_931372.2:n.316-6534A=
XR_931373.2:n.318-54A=
NM_000834.5:c.2010+39T= MANE Select NP_000825.2:n.2010+39T=